{"title":"Proteins","description":"","products":[{"product_id":"rps6-antibody-sc-f0163","title":"S6 Ribosomal Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eRibosomal protein S6(rpS6) is one of the ribosomal proteins of the 40S subunit of eukaryotic ribosomes, weighing in at ≈34 kDa, located near the tRNA\/mRNA binding site. This protein has five phosphorylatable serine residues (Ser235, Ser236, Ser240, Ser244, and Ser247) in the region close to the carboxy terminus. Depending on the literature source, RPS6 may also be discussed as S6 Ribosomal Protein and Ribosomal Protein S6.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following RPS6 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRPS6 is commonly interpreted in the context of cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for RPS6. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in RPS6 reflect biology rather than handling. When interpreting RPS6, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep RPS6 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577387032921,"sku":"F0163-20UL","price":139.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577387065689,"sku":"F0163-100UL","price":329.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577387098457,"sku":"F0163-2X100UL","price":489.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F0163-IF.png?v=1773598160"},{"product_id":"rps6-antibody-sc-f0198","title":"Phospho-S6 Ribosomal Protein (S235\/236) Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eRPS6 is a target of interest in many antibody-based workflows. Growth factors and mitogens effectively stimulate sustained cell growth and proliferation by upregulating mRNA translation. Activation of p70 S6 kinase and subsequent phosphorylation of S6 ribosomal protein are key events in this process. Phosphorylation of S6 ribosomal protein leads to enhanced translation of mRNA transcripts containing an oligopyrimidine tract in their 5' untranslated regions. Depending on the literature source, RPS6 may also be discussed as Phospho-S6 Ribosomal Protein (S235\/236) and Phospho-S6 Ribosomal Protein (Ser235\/236).\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following RPS6 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRPS6 is commonly interpreted in the context of metabolism research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003eresponses linked to nutrient status, mitochondrial state, or metabolic rewiring\u003c\/li\u003e\n\u003cli\u003edifferences between total target abundance and site-specific regulation when modified forms are compared\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for RPS6. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in RPS6 reflect biology rather than handling. When interpreting RPS6, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep RPS6 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577424290137,"sku":"F0198-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577424322905,"sku":"F0198-100UL","price":419.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577424355673,"sku":"F0198-2X100UL","price":629.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F0198-IF.png?v=1773598195"},{"product_id":"rps6-antibody-sc-f0303","title":"Phospho-S6 Ribosomal Protein (Ser240\/244) Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eRPS6 is a target of interest in many antibody-based workflows. To facilitate cell division, mitogens stimulate mRNA translation by activating p70 S6 kinase, leading to phosphorylation of S6 ribosomal protein. This phosphorylation enhances translation of mRNA transcripts containing an oligopyrimidine tract in their 5' untranslated regions, encoding proteins crucial for cell cycle progression, ribosomal proteins, and translation factors. Depending on the literature source, RPS6 may also be discussed as Phospho-S6 Ribosomal Protein (Ser240\/244) and RPS6 (phospho S240 + S244).\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following RPS6 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRPS6 is commonly interpreted in the context of developmental biology research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003estage-dependent patterns during differentiation, morphogenesis, or lineage commitment\u003c\/li\u003e\n\u003cli\u003edifferences between total target abundance and site-specific regulation when modified forms are compared\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for RPS6. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in RPS6 reflect biology rather than handling. When interpreting RPS6, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep RPS6 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577439854937,"sku":"F0303-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577439887705,"sku":"F0303-100UL","price":419.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577439920473,"sku":"F0303-2X100UL","price":629.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F0303-IHC1.jpg?v=1773598310"},{"product_id":"ptx1-antibody-sc-f1024","title":"C Reactive Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003ePTX1 is a target of interest in many antibody-based workflows. C-reactive protein (CRP) is a highly conserved, homopentameric plasma protein classified as an acute-phase inflammatory marker. During infection or inflammation, CRP levels can increase dramatically-by as much as 1,000-fold. In the presence of calcium, CRP binds to phosphocholine (PCh) and other polysaccharide structures found on microbial surfaces, initiating the classical complement cascade by interacting with C1q, thereby contributing to innate immune defense. Depending on the literature source, PTX1 may also be discussed as C Reactive Protein and CRP.\u003c\/p\u003e\u003cp\u003eReported cellular context includes secreted, which can matter when signal is compared across treatments or changing cell states. Following PTX1 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003ePTX1 is commonly interpreted in the context of immunology, inflammation, and cardiovascular research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans secreted, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003esignal enrichment within secreted relative to the broader cellular background\u003c\/li\u003e\n\u003cli\u003econtext differences tied to immune-cell state, activation, or lineage composition\u003c\/li\u003e\n\u003cli\u003eresponses associated with cytokine exposure, inflammatory tone, or tissue stress\u003c\/li\u003e\n\u003cli\u003echanges linked to vascular, contractile, or hemodynamic cell-state cues\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for PTX1. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in PTX1 reflect biology rather than handling. When interpreting PTX1, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep PTX1 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577592193369,"sku":"F1024-20UL","price":149.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577592226137,"sku":"F1024-100UL","price":329.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577592258905,"sku":"F1024-2X100UL","price":489.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1024-wb.gif?v=1773599201"},{"product_id":"cd243-antibody-sc-f1045","title":"P Glycoprotein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eCD243 is a target of interest in many antibody-based workflows. Permeability glycoprotein (P-glycoprotein, Pgp) is a transmembrane protein weighing 170 kD, encoded by the multidrug resistance gene 1 (MDR-1), also referred to as the adenosine triphosphate binding cassette B1 gene (ABCB1). It is located on chromosome 7. This protein is responsible for the resistance to drugs used in chemotherapy, human immunodeficiency virus (HIV) therapy, epilepsy, and inflammatory bowel disease (IBD). Depending on the literature source, CD243 may also be discussed as P Glycoprotein and MDR1.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell membrane, which can matter when signal is compared across treatments or changing cell states. Following CD243 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eCD243 is commonly interpreted in the context of immunology research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cell membrane, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003esignal enrichment within cell membrane relative to the broader cellular background\u003c\/li\u003e\n\u003cli\u003econtext differences tied to immune-cell state, activation, or lineage composition\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for CD243. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in CD243 reflect biology rather than handling. When interpreting CD243, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep CD243 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577596551513,"sku":"F1045-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577596584281,"sku":"F1045-100UL","price":329.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577596617049,"sku":"F1045-2X100UL","price":489.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1045-IHC1.jpg?v=1773599219"},{"product_id":"mbp-antibody-sc-f1098","title":"Myelin Basic Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eMyelin basic protein (MBP) is a protein that lacks a defined structure and shares characteristics with other proteins involved in signal transduction, cell cycle regulation, and those associated with microtubules. It is the second most abundant protein found in the myelin of the central nervous system, responsible for the adhesion of the cytosolic surfaces of multilayered compact myelin. Depending on the literature source, MBP may also be discussed as Myelin Basic Protein.\u003c\/p\u003e\u003cp\u003eReported cellular context includes myelin membrane, cytoplasm, and nucleus, which can matter when signal is compared across treatments or changing cell states. Following MBP across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eMBP is commonly interpreted in the context of neuroscience research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans myelin membrane, cytoplasm, and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between myelin membrane, cytoplasm, and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003ecompartment-specific patterns relevant to neuronal polarity, transport, or synaptic context\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for MBP. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in MBP reflect biology rather than handling. When interpreting MBP, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep MBP trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577610608985,"sku":"F1098-20UL","price":149.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577610641753,"sku":"F1098-100UL","price":359.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577610674521,"sku":"F1098-2X100UL","price":539.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1098-IF.png?v=1773599286"},{"product_id":"nuclear-pore-complex-proteins-antibody-sc-f1538","title":"Nuclear Pore Complex Proteins Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eNuclear Pore Complex Proteins is a target of interest in many antibody-based workflows. Nuclear pore complexes (NPCs) are large structures composed of multiple copies of approximately 30 distinct proteins known as nucleoporins (Nups). Each NPC is assembled from these Nups, which are organized in an octagonal symmetry around a central transport channel. NPCs span the nuclear envelope (NE) and serve as gatekeepers, regulating the transport of macromolecules between the nucleus and the cytoplasm.\u003c\/p\u003e\u003cp\u003eReported cellular context includes nucleus, chromosome, centromere, and kinetochore, which can matter when signal is compared across treatments or changing cell states. Following Nuclear Pore Complex Proteins across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eNuclear Pore Complex Proteins is commonly interpreted in the context of cell cycle and cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans nucleus, chromosome, and centromere, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between nucleus, chromosome, and centromere across matched conditions\u003c\/li\u003e\n\u003cli\u003ecell-cycle linked differences in abundance, timing, or compartmental enrichment\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for Nuclear Pore Complex Proteins. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in Nuclear Pore Complex Proteins reflect biology rather than handling. When interpreting Nuclear Pore Complex Proteins, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep Nuclear Pore Complex Proteins trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577770418521,"sku":"F1538-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577770451289,"sku":"F1538-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577770484057,"sku":"F1538-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1538-IF.png?v=1773599847"},{"product_id":"uqcrc1-antibody-sc-f1582","title":"Ubiquinol-Cytochrome C Reductase Core Protein I Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eUbiquinol-cytochrome c reductase core protein 1 (UQCRC1) is a core component of the mitochondrial ubiquinol-cytochrome c reductase complex (also known as the cytochrome bc1 complex or complex III), which is responsible for transferring electrons from coenzyme Q to cytochrome c, coupled with proton translocation across the inner mitochondrial membrane. This complex consists of 11 subunits, among which UQCRC1 is associated with cytochrome c to prevent apoptosis, and suppressing cytochrome c expression restores UQCRC1-mediated neurodegeneration. Depending on the literature source, UQCRC1 may also be discussed as Ubiquinol-Cytochrome C Reductase Core Protein I.\u003c\/p\u003e\u003cp\u003eReported cellular context includes mitochondrion inner membrane and cell membrane, which can matter when signal is compared across treatments or changing cell states. Following UQCRC1 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eUQCRC1 is commonly interpreted in the context of apoptosis and cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans mitochondrion inner membrane and cell membrane, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between mitochondrion inner membrane and cell membrane across matched conditions\u003c\/li\u003e\n\u003cli\u003eseparation of survival-associated changes from stress or death-associated readouts\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for UQCRC1. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in UQCRC1 reflect biology rather than handling. When interpreting UQCRC1, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep UQCRC1 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577783460185,"sku":"F1582-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577783492953,"sku":"F1582-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577783525721,"sku":"F1582-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1582-IF.png?v=1773599904"},{"product_id":"wt1-antibody-sc-f1596","title":"Wilms Tumor Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eWilms Tumor Protein (WT1) is a transcription factor encoded by the WT1 gene on chromosome 11p13. It binds DNA through four zinc fingers, specifically to the consensus sequence 5′-GCGGGGGCG-3′, similar to EGR1. WT1 functions in transcriptional regulation and post-transcriptional roles via RNA interactions, playing crucial roles in the development and homeostasis of gonads, adrenal glands, kidneys, heart, and diaphragm, where it is involved in MET and EMT processes. Depending on the literature source, WT1 may also be discussed as Wilms Tumor Protein.\u003c\/p\u003e\u003cp\u003eReported cellular context includes nucleus and cytoplasm, which can matter when signal is compared across treatments or changing cell states. Following WT1 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eWT1 is commonly interpreted in the context of cancer, developmental biology, and cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans nucleus and cytoplasm, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between nucleus and cytoplasm across matched conditions\u003c\/li\u003e\n\u003cli\u003echanges associated with proliferative state, oncogenic signaling, or treatment response\u003c\/li\u003e\n\u003cli\u003estage-dependent patterns during differentiation, morphogenesis, or lineage commitment\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for WT1. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in WT1 reflect biology rather than handling. When interpreting WT1, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep WT1 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577789194585,"sku":"F1596-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577789227353,"sku":"F1596-100UL","price":379.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577789260121,"sku":"F1596-2X100UL","price":569.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F1596-IF.png?v=1773599918"},{"product_id":"nuclear-matrix-protein-p84-antibody-sc-f2246","title":"Nuclear Matrix Protein p84 Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eThe nuclear matrix protein p84, also known as THOC1, serves as a critical binding partner for the amino-terminal region of the retinoblastoma (RB) protein, specifically in its hypophosphorylated, growth-suppressive state. This interaction is vital as p84 is primarily localized in subnuclear regions involved in RNA processing and transcription, enabling it to anchor RB to these functionally active nuclear domains.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following Nuclear Matrix Protein p84 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eNuclear Matrix Protein p84 is commonly interpreted in the context of cancer research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003echanges associated with proliferative state, oncogenic signaling, or treatment response\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for Nuclear Matrix Protein p84. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in Nuclear Matrix Protein p84 reflect biology rather than handling. When interpreting Nuclear Matrix Protein p84, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep Nuclear Matrix Protein p84 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577904865625,"sku":"F2246-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577904898393,"sku":"F2246-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577904931161,"sku":"F2246-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F2246-IF.png?v=1773600300"},{"product_id":"protein-casp-antibody-sc-f2405","title":"Protein CASP Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eProtein CASP, also known as CUX1 (Cut-like homeobox 1) is a transcription factor that plays a complex and context-dependent role in cellular functions, development, and disease, with multiple isoforms, including the p110 and p75 variants, produced through alternative splicing and proteolytic processing. These isoforms play distinct roles in regulating gene expression, cell differentiation, proliferation, migration, and invasion.\u003c\/p\u003e\u003cp\u003eReported cellular context includes golgi apparatus and membrane, which can matter when signal is compared across treatments or changing cell states. Following Protein CASP across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eProtein CASP is commonly interpreted in the context of cancer, developmental biology, and apoptosis research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans golgi apparatus and membrane, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between golgi apparatus and membrane across matched conditions\u003c\/li\u003e\n\u003cli\u003echanges associated with proliferative state, oncogenic signaling, or treatment response\u003c\/li\u003e\n\u003cli\u003estage-dependent patterns during differentiation, morphogenesis, or lineage commitment\u003c\/li\u003e\n\u003cli\u003eseparation of survival-associated changes from stress or death-associated readouts\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for Protein CASP. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in Protein CASP reflect biology rather than handling. When interpreting Protein CASP, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep Protein CASP trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577935896921,"sku":"F2405-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577935929689,"sku":"F2405-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577935962457,"sku":"F2405-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F2405-IF.png?v=1773600372"},{"product_id":"fr-alpha-antibody-sc-f2457","title":"Folate Binding Protein \/ FBP Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eFR-ALPHA is a target of interest in many antibody-based workflows. Folate binding protein (FBP), also known as folate receptor (FR), is a high-affinity glycoprotein that binds folic acid and its analogues and exists in both membrane-bound and soluble forms. It is primarily expressed in limited normal tissues such as kidney proximal tubules, placenta, and intestinal mucosa, but is significantly overexpressed in many epithelial cancers including ovarian, endometrial, breast, and lung cancers. Depending on the literature source, FR-ALPHA may also be discussed as Folate Binding Protein \/ FBP and Folate receptor alpha.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell membrane, cytoplasmic vesicle, endosome, and membrane, which can matter when signal is compared across treatments or changing cell states. Following FR-ALPHA across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eFR-ALPHA is commonly interpreted in the context of cancer and immunology research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cell membrane, cytoplasmic vesicle, and endosome, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cell membrane, cytoplasmic vesicle, and endosome across matched conditions\u003c\/li\u003e\n\u003cli\u003echanges associated with proliferative state, oncogenic signaling, or treatment response\u003c\/li\u003e\n\u003cli\u003econtext differences tied to immune-cell state, activation, or lineage composition\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for FR-ALPHA. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in FR-ALPHA reflect biology rather than handling. When interpreting FR-ALPHA, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep FR-ALPHA trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577951920473,"sku":"F2457-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577951953241,"sku":"F2457-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577951986009,"sku":"F2457-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F2457-wb.gif?v=1773600419"},{"product_id":"sp-c-antibody-sc-f2479","title":"Prosurfactant Protein C Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eProsurfactant protein C (proSP-C) is a 197-residue integral membrane protein in the endoplasmic reticulum (ER), where its transmembrane (TM) region forms the mature surfactant protein C (SP-C). The C-terminal domain (CTC, residues 59-197), located in the ER lumen, contains a Brichos domain (residues 94-197) that plays a crucial role in preventing amyloid formation of the poly-Val TM region during biosynthesis. Depending on the literature source, SP-C may also be discussed as Prosurfactant Protein C and proSP-C.\u003c\/p\u003e\u003cp\u003eReported cellular context includes secreted and surface film, which can matter when signal is compared across treatments or changing cell states. Following SP-C across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eSP-C is commonly interpreted in the context of metabolism research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans secreted and surface film, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between secreted and surface film across matched conditions\u003c\/li\u003e\n\u003cli\u003eresponses linked to nutrient status, mitochondrial state, or metabolic rewiring\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for SP-C. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in SP-C reflect biology rather than handling. When interpreting SP-C, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep SP-C trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577953952089,"sku":"F2479-20UL","price":199.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577953984857,"sku":"F2479-100UL","price":489.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577954017625,"sku":"F2479-2X100UL","price":729.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/f2479-IHC1.jpg?v=1773600446"},{"product_id":"app-antibody-sc-f2535","title":"Amyloid Precursor Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eAmyloid Precursor Protein (APP) is a type I transmembrane glycoprotein primarily expressed in the brain, concentrated at neuronal synapses, and involved in critical cellular functions, including synaptogenesis, neuronal growth, synaptic plasticity, and survival. APP consists of a large extracellular N-terminal domain with subdomains like the growth factor-like domain (GFLD) and copper-binding domain (CuBD), a single transmembrane α-helix, and a short intracellular C-terminal domain containing conserved motifs such as YENPTY for intracellular signalling and trafficking. Depending on the literature source, APP may also be discussed as Amyloid Precursor Protein and C-Terminal.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell membrane, cell projection, coated pit, and cytoplasm, which can matter when signal is compared across treatments or changing cell states. Following APP across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eAPP is commonly interpreted in the context of neuroscience research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cell membrane, cell projection, and coated pit, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cell membrane, cell projection, and coated pit across matched conditions\u003c\/li\u003e\n\u003cli\u003ecompartment-specific patterns relevant to neuronal polarity, transport, or synaptic context\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003cli\u003etime-matched comparisons so changes reflect biology rather than handling or sampling drift\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for APP. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in APP reflect biology rather than handling. When interpreting APP, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep APP trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577958768985,"sku":"F2535-20UL","price":169.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577958801753,"sku":"F2535-100UL","price":399.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577958834521,"sku":"F2535-2X100UL","price":599.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F2535-IF.png?v=1773600518"},{"product_id":"prkra-antibody-sc-f2996","title":"PACT (PKR activating protein) \/ PRKRA Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003ePACT (PKR activating protein)\/PRKRA, also known as (Protein Activator of PKR) is a 313-amino acid cellular protein characterized by three conserved double-stranded RNA-binding motifs (dsRBMs), of which dsRBMs 1 and 2 bind dsRNA, while domain 3 is crucial for activating the double-stranded RNA-activated protein kinase (PKR) in vitro, even in the absence of dsRNA. PACT is widely expressed, with high levels in the brain and immune cells, and its expression is upregulated by factors like proinflammatory cytokines, stress conditions (oxidative or hyperosmotic), and viral infections. Depending on the literature source, PRKRA may also be discussed as PACT (PKR activating protein) \/ PRKRA and PACT.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm, which can matter when signal is compared across treatments or changing cell states. Following PRKRA across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003ePRKRA is commonly interpreted in the context of immunology and infectious disease research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003esignal enrichment within cytoplasm relative to the broader cellular background\u003c\/li\u003e\n\u003cli\u003econtext differences tied to immune-cell state, activation, or lineage composition\u003c\/li\u003e\n\u003cli\u003ehost-response changes during infection or pathogen-associated stimulation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for PRKRA. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in PRKRA reflect biology rather than handling. When interpreting PRKRA, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep PRKRA trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57577990422873,"sku":"F2996-20UL","price":149.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577990455641,"sku":"F2996-100UL","price":329.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577990488409,"sku":"F2996-2X100UL","price":489.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F2996-wb.gif?v=1773600873"},{"product_id":"ribosomal-protein-s3-antibody-sc-f3047","title":"Ribosomal Protein S3 Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eRibosomal protein S3 (RPS3) is a component of the eukaryotic 40S ribosomal subunit, playing crucial roles beyond its involvement in protein synthesis. RPS3 features an N-terminal domain responsible for protein-protein interactions and binding ribosomal RNA (rRNA), facilitating ribosome assembly. It can dimerize and associate with chaperones during its nuclear import.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm, cytoskeleton, membrane, and mitochondrion, which can matter when signal is compared across treatments or changing cell states. Following Ribosomal Protein S3 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRibosomal Protein S3 is commonly interpreted in the context of inflammation and infectious disease research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm, cytoskeleton, and membrane, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm, cytoskeleton, and membrane across matched conditions\u003c\/li\u003e\n\u003cli\u003eresponses associated with cytokine exposure, inflammatory tone, or tissue stress\u003c\/li\u003e\n\u003cli\u003ehost-response changes during infection or pathogen-associated stimulation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for Ribosomal Protein S3. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in Ribosomal Protein S3 reflect biology rather than handling. When interpreting Ribosomal Protein S3, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep Ribosomal Protein S3 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57578000712025,"sku":"F3047-20UL","price":149.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57578000744793,"sku":"F3047-100UL","price":359.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57578000777561,"sku":"F3047-2X100UL","price":539.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F3047-IF.png?v=1773600909"},{"product_id":"rps6-antibody-sc-f3521","title":"S6 Ribosomal Protein Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eRibosomal Protein S6 (RPS6) is a highly conserved protein and a core component of the 40S small ribosomal subunit in eukaryotes, classified within the S6E family of ribosomal proteins. Comprising approximately 249 amino acids (~28. 6 kDa), RPS6 plays a pivotal role in the regulation of protein synthesis, cell growth, and proliferation. Depending on the literature source, RPS6 may also be discussed as S6 Ribosomal Protein and Small ribosomal subunit protein eS6; 40S ribosomal protein S6; Phosphoprotein NP33; RPS6; OK\/SW-cl.2.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following RPS6 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRPS6 is commonly interpreted in the context of metabolism and cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003eresponses linked to nutrient status, mitochondrial state, or metabolic rewiring\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003cli\u003eco-patterning with orthogonal markers and control conditions that clarify pathway state\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for RPS6. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in RPS6 reflect biology rather than handling. When interpreting RPS6, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep RPS6 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57578028794201,"sku":"F3521-20UL","price":139.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57578028826969,"sku":"F3521-100UL","price":339.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57578028859737,"sku":"F3521-2X100UL","price":499.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F3521-IF.png?v=1773601284"},{"product_id":"rps6-antibody-sc-f3530","title":"Phospho-S6 Ribosomal Protein (S235\/236) Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003ePhospho-S6 Ribosomal Protein (Ser235\/236) is the phosphorylated form of ribosomal protein S6 (RPS6), a 249-amino acid (~28. 6 kDa) protein and essential component of the 40S small ribosomal subunit within the S6E family. RPS6 plays a central role in regulating protein synthesis and cell growth, with phosphorylation occurring primarily at serine residues 235 and 236 in its carboxy-terminal region. Depending on the literature source, RPS6 may also be discussed as Phospho-S6 Ribosomal Protein (S235\/236) and Small ribosomal subunit protein eS6; 40S ribosomal protein S6; Phosphoprotein NP33; RPS6; OK\/SW-cl.2.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cytoplasm and nucleus, which can matter when signal is compared across treatments or changing cell states. Following RPS6 across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eRPS6 is commonly interpreted in the context of neuroscience, metabolism, and cell signaling research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans cytoplasm and nucleus, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.\u003c\/p\u003e\u003cp\u003eConsider these angles when interpreting target-level changes:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eapparent redistribution between cytoplasm and nucleus across matched conditions\u003c\/li\u003e\n\u003cli\u003ecompartment-specific patterns relevant to neuronal polarity, transport, or synaptic context\u003c\/li\u003e\n\u003cli\u003eresponses linked to nutrient status, mitochondrial state, or metabolic rewiring\u003c\/li\u003e\n\u003cli\u003esignal-dependent shifts after ligand, inhibitor, or growth-factor perturbation\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for RPS6. This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.\u003c\/p\u003e\u003cp\u003eStandardize sampling time, control choice, and downstream analysis thresholds so apparent differences in RPS6 reflect biology rather than handling. When interpreting RPS6, it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, a shared reference condition can keep RPS6 trends easier to compare across datasets. That kind of consistency is especially helpful when follow-up work expands to new perturbations, model systems, or longitudinal collections.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"20 µl","offer_id":57578029056345,"sku":"F3530-20UL","price":189.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57578029089113,"sku":"F3530-100UL","price":389.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57578029121881,"sku":"F3530-2X100UL","price":589.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F3530-IF.png?v=1773601287"},{"product_id":"myelin-oligodendrocyte-glycoprotein-35-55-mouse-rat-p1204","title":"Myelin Oligodendrocyte Glycoprotein 35-55 (Mouse, Rat)","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eMyelin Oligodendrocyte Glycoprotein 35-55, mouse, rat (MOG 35-55) is a minor component of CNS myelin that induces experimental autoimmune encephalomyelitis in C57BL\/6 mice by an encephalitogenic T cell response. The mapped biological anchor for this entry is Myelin oligodendrocyte glycoprotein (source antigen) (MOG), although the description suggests that interpretation should remain at fragment, family, or pathway level. Here the product is best viewed as a defined fragment or protein-derived reagent, which helps isolate aggregation behavior, antigenicity, binding interfaces, or stress-related biology from the full-length precursor context. Researchers commonly study this context in immunology settings, where perturbation can reshape cytokine output, leukocyte activation state, and inflammatory remodeling. This framing is especially useful when investigators need a defined fragment model rather than the full-length precursor context.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eBecause it is an antigenic fragment, this reagent is usually used to model epitope-specific recognition or disease-associated immune activation rather than receptor pharmacology. In practice, handling conditions, timing, and matched controls are important for separating fragment-dependent effects from responses driven by broader precursor or pathway biology. When species annotation matters, keeping comparisons within the stated mouse; rat context helps reduce ambiguity in receptor or sequence preference. Because the enrichment is not fully single-target, conclusions are usually strongest when they are framed around the intended biological process and confirmed with orthogonal markers.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003etreat the reagent as a defined fragment model rather than as a full-length-protein substitute\u003c\/li\u003e\n\u003cli\u003econtrol handling conditions that can influence aggregation state, epitope presentation, or interface exposure\u003c\/li\u003e\n\u003cli\u003einterpret downstream phenotypes together with assays that confirm the relevant fragment-dependent state\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eExperimental interpretation should therefore connect early pathway changes with later phenotypic outputs, rather than relying on a single endpoint in isolation.\u003c\/p\u003e\u003ch2\u003eFormat Considerations\u003c\/h2\u003e\u003cp\u003eUsing the regular format helps keep comparative experiments aligned, especially when the same signaling question is being tested across multiple models or readout platforms. In comparative workflows, retaining the annotated mouse; rat species context helps when comparing sequence-dependent biology. This is particularly helpful for comparative experiments, benchmark studies, and orthogonal validation in which small differences in formulation or handling can complicate interpretation. For peptide-centered workflows, conclusions are usually strongest when biological readouts are paired with consistent preparation and appropriately matched reference conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"5 mg","offer_id":57636821303641,"sku":"P1204-5MG","price":254.0,"currency_code":"EUR","in_stock":true},{"title":"25 mg","offer_id":57636821336409,"sku":"P1204-25MG","price":763.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/p1204-mog-35-55--chemical-structure.gif?v=1774212356"},{"product_id":"proteinase-k-p1242","title":"Proteinase K","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eProteinase K is a serine endoprotease, is used for isolating amyloid cores and is effective over a wide pH range (4–12), including in the presence of SDS or urea. This entry is best interpreted as a functional research reagent rather than as a strictly single-target ligand. For these entries, interpretation usually centers on how the material affects assay conditions or functional biology rather than on exclusive engagement of a single genetically defined receptor or enzyme. In workflow-oriented studies, investigators often focus on sample quality, assay background, and biochemical workflow performance. In practical terms, the product supports reproducible workflows in which matched preparation conditions are central to interpretation.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eAs an enzyme reagent, it is usually interpreted through sample-processing utility or broad proteolytic activity rather than receptor-selective signaling. In practice, preparation, concentration, contact time, and matched workflow controls are important for separating material effects from biological signal. Because the enrichment is not fully single-target, conclusions are usually strongest when they are framed around the intended biological process and confirmed with orthogonal markers.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003emaintain matched workflow conditions so changes in assay background are not mistaken for target biology\u003c\/li\u003e\n\u003cli\u003einterpret results at the functional or systems level rather than as evidence of exclusive single-target binding\u003c\/li\u003e\n\u003cli\u003euse consistent preparation, exposure, and handling steps across comparative experiments\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eExperimental interpretation should therefore connect early pathway changes with later phenotypic outputs, rather than relying on a single endpoint in isolation.\u003c\/p\u003e\u003ch2\u003eFormat Considerations\u003c\/h2\u003e\u003cp\u003eThe standard product format is most useful for reproducible baseline experiments, matched comparative studies, and workflows that need a consistent reagent across assay repeats. In comparative workflows, consistency of preparation, exposure window, and matched controls is often as important as the nominal treatment itself. This is particularly helpful for comparative experiments, benchmark studies, and orthogonal validation in which small differences in formulation or handling can complicate interpretation. For peptide-centered workflows, conclusions are usually strongest when biological readouts are paired with consistent preparation and appropriately matched reference conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"5 mg","offer_id":57636822679897,"sku":"P1242-5MG","price":193.0,"currency_code":"EUR","in_stock":true},{"title":"25 mg","offer_id":57636822712665,"sku":"P1242-25MG","price":488.0,"currency_code":"EUR","in_stock":true},{"title":"100 mg","offer_id":57636822745433,"sku":"P1242-100MG","price":953.0,"currency_code":"EUR","in_stock":true},{"title":"1 g","offer_id":57636822778201,"sku":"P1242-1G","price":2918.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/P1242-Proteinase-K-chemical-structure-tube.png?v=1774212392"},{"product_id":"anti-lcmv-np-antibody-vl-4","title":"Anti-LCMV nucleoprotein - InVivo","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eFor consistent comparison across experiments, use this antibody to investigate LCMV nucleoprotein with a repeatable workflow. LCMV nucleoprotein is frequently evaluated in infectious disease where researchers compare target-linked changes across matched conditions, perturbations, and model systems. Using shared controls and stable handling criteria helps keep observed differences interpretable as studies expand.\u003c\/p\u003e\u003cp\u003eIn infectious disease settings, timing of exposure, host-response state, and sampling windows can strongly influence the way LCMV nucleoprotein-linked signals are interpreted. Following LCMV nucleoprotein across replicate sets can help separate abundance-related changes from effects driven by localization, cell-state composition, or treatment timing.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eBecause target-associated signal can vary with sampling window, matrix, and biological context, experimental design usually benefits from predefined controls and consistent inclusion criteria. This is especially important when LCMV nucleoprotein is studied across multiple perturbations, response states, or longitudinal collections.\u003c\/p\u003e\u003cp\u003eWhen interpreting LCMV nucleoprotein, it can be useful to compare direct target readouts with companion markers that anchor pathway activity, cell identity, or sample quality. That approach makes it easier to distinguish a true biological shift from processing-related variation or background differences between runs.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003ebaseline abundance versus context-dependent redistribution\u003c\/li\u003e\n\u003cli\u003etreatment timing or stimulation effects on signal intensity\u003c\/li\u003e\n\u003cli\u003eco-occurrence with pathway or lineage markers in matched samples\u003c\/li\u003e\n\u003cli\u003ehost-response versus pathogen-linked contributions to the readout\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular format offers a balanced option for establishing baseline signal behavior for LCMV nucleoprotein. This matters because extraction, incubation, and detection conditions can all influence apparent readout strength even when the underlying biology is unchanged.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, it helps to define a shared reference condition for LCMV nucleoprotein early in the workflow so cross-sample contrasts remain meaningful. Matched processing and stable review criteria reduce the chance that workflow drift will be mistaken for a target-linked biological effect.\u003c\/p\u003e\u003cp\u003eAcross independent experiments, standardized handling supports more reliable interpretation of LCMV nucleoprotein in comparative datasets, whether the goal is screening, mechanism-focused follow-up, or confirmation across related models.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"1 mg","offer_id":57770720624985,"sku":"A2146-1MG","price":149.0,"currency_code":"EUR","in_stock":true},{"title":"5 mg","offer_id":57770720657753,"sku":"A2146-5MG","price":539.0,"currency_code":"EUR","in_stock":true},{"title":"5 × 5 mg","offer_id":57770720690521,"sku":"A2146-5X1MG","price":1749.0,"currency_code":"EUR","in_stock":true},{"title":"20 × 5 mg","offer_id":57770720723289,"sku":"A2146-20X5MG","price":3590.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"anti-melanotransferrin-antibody","title":"Anti-Melanotransferrin \/ CD228","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eFor consistent comparison across experiments, use this antibody to investigate CD228 with a repeatable workflow. CD228 is frequently evaluated in immunology where researchers compare target-linked changes across matched conditions, perturbations, and model systems. Using shared controls and stable handling criteria helps keep observed differences interpretable as studies expand.\u003c\/p\u003e\u003cp\u003eIn immune-focused studies, CD228 is often interpreted alongside cell-state composition, activation timing, and cytokine exposure. Following CD228 across replicate sets can help separate abundance-related changes from effects driven by localization, cell-state composition, or treatment timing.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eBecause target-associated signal can vary with sampling window, matrix, and biological context, experimental design usually benefits from predefined controls and consistent inclusion criteria. This is especially important when CD228 is studied across multiple perturbations, response states, or longitudinal collections.\u003c\/p\u003e\u003cp\u003eWhen interpreting CD228, it can be useful to compare direct target readouts with companion markers that anchor pathway activity, cell identity, or sample quality. That approach makes it easier to distinguish a true biological shift from processing-related variation or background differences between runs.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003ecell-state composition versus target-specific signal changes\u003c\/li\u003e\n\u003cli\u003eactivation timing, cytokine exposure, or checkpoint-dependent effects\u003c\/li\u003e\n\u003cli\u003eco-occurrence with pathway or lineage markers in matched samples\u003c\/li\u003e\n\u003cli\u003edifferences between biological response and technical background\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular format offers a balanced option for establishing baseline signal behavior for CD228. This matters because extraction, incubation, and detection conditions can all influence apparent readout strength even when the underlying biology is unchanged.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, it helps to define a shared reference condition for CD228 early in the workflow so cross-sample contrasts remain meaningful. Matched processing and stable review criteria reduce the chance that workflow drift will be mistaken for a target-linked biological effect.\u003c\/p\u003e\u003cp\u003eAcross independent experiments, standardized handling supports more reliable interpretation of CD228 in comparative datasets, whether the goal is screening, mechanism-focused follow-up, or confirmation across related models.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"1 mg","offer_id":57770758046041,"sku":"A2402-1MG","price":529.0,"currency_code":"EUR","in_stock":true},{"title":"5 × 1 mg","offer_id":57770758078809,"sku":"A2402-5X1MG","price":1660.0,"currency_code":"EUR","in_stock":true},{"title":"25 × 1 mg","offer_id":57770758111577,"sku":"A2402-25X1MG","price":4982.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"anti-gp6-antibody-glenzocimab","title":"Glenzocimab (Anti-GP6 \/ Glycoprotein-6)","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eFor consistent comparison across experiments, use this antibody to investigate GP6 with a repeatable workflow. GP6 is frequently evaluated in target-focused research where researchers compare target-linked changes across matched conditions, perturbations, and model systems. Using shared controls and stable handling criteria helps keep observed differences interpretable as studies expand.\u003c\/p\u003e\u003cp\u003eGP6 is often examined in comparative workflows where investigators want a repeatable way to track target-associated changes across matched experimental conditions. Following GP6 across replicate sets can help separate abundance-related changes from effects driven by localization, cell-state composition, or treatment timing.\u003c\/p\u003e\u003ch2\u003eResearch Context\u003c\/h2\u003e\u003cp\u003eBecause target-associated signal can vary with sampling window, matrix, and biological context, experimental design usually benefits from predefined controls and consistent inclusion criteria. This is especially important when GP6 is studied across multiple perturbations, response states, or longitudinal collections.\u003c\/p\u003e\u003cp\u003eWhen interpreting GP6, it can be useful to compare direct target readouts with companion markers that anchor pathway activity, cell identity, or sample quality. That approach makes it easier to distinguish a true biological shift from processing-related variation or background differences between runs.\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003ebaseline abundance versus context-dependent redistribution\u003c\/li\u003e\n\u003cli\u003etreatment timing or stimulation effects on signal intensity\u003c\/li\u003e\n\u003cli\u003eco-occurrence with pathway or lineage markers in matched samples\u003c\/li\u003e\n\u003cli\u003edifferences between biological response and technical background\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eVariant Considerations\u003c\/h2\u003e\u003cp\u003eIf your project spans exploratory questions, the regular format offers a balanced option for establishing baseline signal behavior for GP6. This matters because extraction, incubation, and detection conditions can all influence apparent readout strength even when the underlying biology is unchanged.\u003c\/p\u003e\u003cp\u003eFor multi-run studies, it helps to define a shared reference condition for GP6 early in the workflow so cross-sample contrasts remain meaningful. Matched processing and stable review criteria reduce the chance that workflow drift will be mistaken for a target-linked biological effect.\u003c\/p\u003e\u003cp\u003eAcross independent experiments, standardized handling supports more reliable interpretation of GP6 in comparative datasets, whether the goal is screening, mechanism-focused follow-up, or confirmation across related models.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"1 mg","offer_id":57770773053785,"sku":"A2478-1MG","price":363.0,"currency_code":"EUR","in_stock":true},{"title":"5 × 1 mg","offer_id":57770773086553,"sku":"A2478-5X1MG","price":953.0,"currency_code":"EUR","in_stock":true},{"title":"25 × 1 mg","offer_id":57770773119321,"sku":"A2478-25X1MG","price":2918.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"irak-4-protein-kinase-inhibitor-2-e0533","title":"IRAK-4 protein kinase inhibitor 2","description":"\u003cp\u003e\u003cstrong\u003eIRAK-4 protein kinase inhibitor 2\u003c\/strong\u003e is an inhibitor of Interleukins used in studies of JAK-STAT Signaling and Immune Signaling. In practice, this places the compound in experiments that measure cytokine-responsive transcriptional signaling and immune regulation and cytokine-mediated signaling and inflammatory effector responses in immunology and inflammation models.\u003c\/p\u003e\n\n\u003cp\u003eBy inhibiting Interleukins, IRAK-4 protein kinase inhibitor 2 can be used to examine cytokine-responsive transcriptional signaling and immune regulation and cytokine-mediated signaling and inflammatory effector responses. The immunomodulator annotation adds relevance to immune-cell activation, cytokine, and mediator assays, together with downstream-response mapping in the same experimental setting. In immunology and inflammation models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.\u003c\/p\u003e\n\n\u003ch2\u003eResearch Applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eTarget-focused assays involving Interleukins\u003c\/li\u003e\n\u003cli\u003ePathway perturbation studies connected to JAK-STAT Signaling and Immune Signaling\u003c\/li\u003e\n\u003cli\u003eConcentration-response inhibition and target-dependence studies\u003c\/li\u003e\n\u003cli\u003eImmune-cell activation, cytokine, and mediator assays\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003eOverall, IRAK-4 protein kinase inhibitor 2 is appropriate when a defined chemical perturbant is needed to connect Interleukins with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in immunology and inflammation models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"5 mg","offer_id":57804277776729,"sku":"E0533-5MG","price":68.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/e0533-irak-4-protein-kinase-inhibitor-2-chemical-structure.gif?v=1776166156"},{"product_id":"transferrins-e7199","title":"Transferrins","description":"\u003cp\u003e\u003cstrong\u003eTransferrins\u003c\/strong\u003e is a research compound linked to Apoptosis and related biological responses. In practice, this places the compound in experiments that measure caspase-associated cell-death signaling and survival decisions in apoptosis and cancer models.\u003c\/p\u003e\n\n\u003cp\u003eThe pathway annotation connects Transferrins to Apoptosis, supporting experiments that monitor caspase-associated cell-death signaling and survival decisions across biochemical, cellular, or phenotypic assay formats. This context is compatible with apoptosis, viability, and caspase-readout assays, as well as transcriptional, biochemical, or phenotypic comparisons linked to the annotated pathway state. In apoptosis and cancer models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.\u003c\/p\u003e\n\n\u003ch2\u003eResearch Applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003ePathway perturbation studies connected to Apoptosis\u003c\/li\u003e\n\u003cli\u003ePhenotypic profiling in apoptosis and cancer models\u003c\/li\u003e\n\u003cli\u003eCombination studies with orthogonal perturbagens\u003c\/li\u003e\n\u003cli\u003eMechanism-oriented follow-up using biochemical and cellular endpoints\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003eOverall, Transferrins is well suited to pathway-oriented studies that need a defined compound input for Apoptosis readouts in apoptosis and cancer models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"5 mg","offer_id":57805039960409,"sku":"E7199-5MG","price":193.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/e7199-transferrins-chemical-structure-tube.png?v=1776171114"},{"product_id":"protein-kinase-c-19-31-e7445","title":"Protein Kinase C (19-31)","description":"\u003cp\u003e\u003cstrong\u003eProtein Kinase C (19-31)\u003c\/strong\u003e is a substrate of PKC used in studies of MAPK \/ ERK Signaling. It is especially relevant in cancer, cell signaling, and immunology models, where defined compound exposure can be linked to mitogenic kinase cascades, proliferation control, and differentiation-linked signaling.\u003c\/p\u003e\n\n\u003cp\u003eAs a substrate linked to PKC, Protein Kinase C (19-31) can be used to examine mitogenic kinase cascades, proliferation control, and differentiation-linked signaling. The kinase annotation adds relevance to biochemical kinase assays, phospho-signaling studies, and selectivity profiling, together with downstream-response mapping in the same experimental setting. In cancer, cell signaling, and immunology models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.\u003c\/p\u003e\n\n\u003ch2\u003eResearch Applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eTarget-focused assays involving PKC\u003c\/li\u003e\n\u003cli\u003ePathway perturbation studies connected to MAPK \/ ERK Signaling\u003c\/li\u003e\n\u003cli\u003eKinetic, turnover, and substrate-competition experiments\u003c\/li\u003e\n\u003cli\u003eBiochemical kinase assays, phospho-signaling studies, and selectivity profiling\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003eOverall, Protein Kinase C (19-31) is appropriate when a defined chemical perturbant is needed to connect PKC with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in cancer, cell signaling, and immunology models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"Default Title","offer_id":57818499645785,"sku":"E7445","price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/e7445-protein-kinase-c-19-31-chemical-structure-tube.png?v=1776275566"},{"product_id":"activated-protein-c-390-404-human-e7617","title":"Activated Protein C (390-404), human","description":"\u003cp\u003e\u003cstrong\u003eActivated Protein C (390-404), human\u003c\/strong\u003e is a research compound associated with Serine Proteases and is relevant to studies of protease biology. In practice, this places the compound in experiments that measure proteolytic processing and cleavage-dependent signaling in inflammation models.\u003c\/p\u003e\n\n\u003cp\u003eThe current annotation links Activated Protein C (390-404), human to Serine Proteases, supporting target-focused studies that measure proteolytic processing and cleavage-dependent signaling without assigning a more specific primary mechanism than the dataset provides. This target class is commonly examined through protease-activity, cleavage, and substrate-processing assays, together with downstream-response mapping. In inflammation models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.\u003c\/p\u003e\n\n\u003ch2\u003eResearch Applications\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eTarget-focused assays involving Serine Proteases\u003c\/li\u003e\n\u003cli\u003eReceptor-binding, peptide-pharmacology, and cell-signaling studies\u003c\/li\u003e\n\u003cli\u003eProtease-activity, cleavage, and substrate-processing assays\u003c\/li\u003e\n\u003cli\u003ePhenotypic profiling in inflammation models\u003c\/li\u003e\n\u003c\/ul\u003e\n\n\u003cp\u003eOverall, Activated Protein C (390-404), human is appropriate when a defined chemical perturbant is needed to connect Serine Proteases with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in inflammation models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.\u003c\/p\u003e","brand":"Selleck Chemicals","offers":[{"title":"Default Title","offer_id":57818622493017,"sku":"E7617","price":0.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/e7617-activated-protein-c-390-404-human-chemical-structure-tube.png?v=1776275746"},{"product_id":"protein-a-g-magnetic-beads","title":"Protein A\/G Magnetic Beads","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eProtein A\/G Magnetic Beads is a research-use reagent supporting western blot workflows. Protein A\/G Magnetic Beads are formed by covalently binding polymer magnetic microspheres with high purity recombinant Protein A\/G. Key notes from the supplied features include: Good binding effects, clear bands, minimal antibody loss (binding efficiency ≥0. To support repeatable purchasing and recordkeeping, the copy reflects the supplied description and features—without overpromising beyond what’s provided.\u003c\/p\u003e\u003ch2\u003eKey Benefits\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eHigh binding capacity:\u003c\/strong\u003e Good binding effects, clear bands, minimal antibody loss (binding efficiency ≥0 for western blot documentation and method consistency.\u003c\/li\u003e\n\u003cli\u003eProtein A\/G Magnetic Beads are formed by covalently binding polymer magnetic microspheres with high purity recombinant Protein A\/G.\u003c\/li\u003e\n\u003cli\u003eThis product has a larger specific surface area and more antibody binding sites, which can greatly shorten the antibody adsorption time and reduce non-specific binding.\u003c\/li\u003e\n\u003cli\u003eClear, structured description for faster review and fewer purchasing errors.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it supports your workflow\u003c\/h2\u003e\u003cp\u003eResearch workflows move faster when the product choice, rationale, and documentation are all in sync—especially for routine assays and repeat ordering. For western blot workflows, the goal is often to keep the scientific rationale and the purchasing record aligned. Protein A\/G Magnetic Beads are formed by covalently binding polymer magnetic microspheres with high purity recombinant Protein A\/G. This product has a larger specific surface area and more antibody binding sites, which can greatly shorten the antibody adsorption time and reduce non-specific binding. The supplied feature set highlights high binding capacity, which can help teams standardize language and expectations across similar products. Because projects evolve, we aim for descriptions that remain searchable, specific, and easy to compare across catalog numbers—so you can reorder confidently and keep documentation consistent. It also helps when you need to hand off a method to a colleague, reference a catalog item in a report, or keep purchasing approvals moving without back-and-forth.\u003c\/p\u003e\u003ch2\u003eApplications \u0026amp; compatibility\u003c\/h2\u003e\u003cp\u003eCompatibility is most useful when it’s stated plainly, so teams can match products to their existing workflows. Based on the supplied information, it’s positioned for western blot workflows where clear documentation and straightforward compatibility notes matter. If you’re matching this item to an established SOP, use the product name, catalog number, and the supplied features as the primary reference points. Use the application notes as a scope guide: they indicate fit and compatibility language drawn from the supplied product information, not assumptions beyond it.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIdeal for:\u003c\/strong\u003e teams building or refining western blot workflows workflows, especially when multiple users need the same language for ordering, reporting, and day-to-day bench notes. Ideal when you need a quick, confident match between what’s on the page and what’s in your records.\u003c\/p\u003e","brand":"Vazyme Biotech","offers":[{"title":"1 ml","offer_id":57911511187801,"sku":"PB101-01","price":105.0,"currency_code":"EUR","in_stock":true},{"title":"5 × 1 ml","offer_id":57911511220569,"sku":"PB101-02","price":380.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/protein-a-g-magnetic-beads.png?v=1777032347"},{"product_id":"250-kda-plus-prestained-protein-marker","title":"250 kDa Plus Prestained Protein Marker","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003e250 kDa Plus Prestained Protein Marker is a research-use reagent supporting western blot workflows. The 250 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 250 kDa. Key notes from the supplied features include: Three-color labelled bandsClear and visibleComponents. The wording is kept close to the supplied product information, helping you reference the right item quickly and document consistently.\u003c\/p\u003e\u003ch2\u003eKey Benefits\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eThree-color labelled bandsClear and visibleComponents.\u003c\/li\u003e\n\u003cli\u003eThe 250 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 250 kDa.\u003c\/li\u003e\n\u003cli\u003eThree different chromophores (orange-red, blue and green) are bound to the proteins, producing a brightly colored marker.\u003c\/li\u003e\n\u003cli\u003eClear, structured description for faster review and fewer purchasing errors.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it supports your workflow\u003c\/h2\u003e\u003cp\u003eIn day-to-day research, teams often need products that fit existing methods while remaining easy to justify in notes, SOPs, and reporting. For western blot workflows, the goal is often to keep the scientific rationale and the purchasing record aligned. The 250 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 250 kDa. Three different chromophores (orange-red, blue and green) are bound to the proteins, producing a brightly colored marker. Because projects evolve, we aim for descriptions that remain searchable, specific, and easy to compare across catalog numbers—so you can reorder confidently and keep documentation consistent. Clear product wording is particularly helpful when you are comparing alternatives, standardizing across projects, or documenting why a specific catalog number was selected. Clear product wording is particularly helpful when you are comparing alternatives, standardizing across projects, or documenting why a specific catalog number was selected.\u003c\/p\u003e\u003ch2\u003eApplications \u0026amp; compatibility\u003c\/h2\u003e\u003cp\u003eUse the notes below to gauge fit for your setup and documentation needs. Based on the supplied information, it’s positioned for western blot workflows where clear documentation and straightforward compatibility notes matter. If you’re matching this item to an established SOP, use the product name, catalog number, and the supplied features as the primary reference points. Use the application notes as a scope guide: they indicate fit and compatibility language drawn from the supplied product information, not assumptions beyond it.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIdeal for:\u003c\/strong\u003e labs focused on western blot workflows; teams that need clear, searchable documentation for purchasing and experimental records; and groups standardizing methods across projects or sites. Ideal when you need a quick, confident match between what’s on the page and what’s in your records.\u003c\/p\u003e","brand":"Vazyme Biotech","offers":[{"title":"100 RXNS","offer_id":57911527965017,"sku":"MP202-01","price":147.0,"currency_code":"EUR","in_stock":true},{"title":"500 RXNS","offer_id":57911527997785,"sku":"MP202-02","price":587.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/250-kda-plus-prestained-protein-marker.png?v=1777032527"},{"product_id":"180-kda-plus-prestained-protein-marker","title":"180 kDa Plus Prestained Protein Marker","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003e180 kDa Plus Prestained Protein Marker is a research-use reagent supporting western blot workflows. The 180 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 180 kDa. Key notes from the supplied features include: Three-color labelled bandsClear and visibleComponents. This listing is anchored to the supplied description and feature set, so your storefront details stay accurate without adding unsupported claims.\u003c\/p\u003e\u003ch2\u003eKey Benefits\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eThree-color labelled bandsClear and visibleComponents for western blot documentation and method consistency.\u003c\/li\u003e\n\u003cli\u003eThe 180 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 180 kDa.\u003c\/li\u003e\n\u003cli\u003eThree different chromophores (orange-red, blue and green) are bound to the proteins, producing a brightly colored marker.\u003c\/li\u003e\n\u003cli\u003eClear, structured description for faster review and fewer purchasing errors.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it supports your workflow\u003c\/h2\u003e\u003cp\u003eWhether you’re validating a result or scaling a method, clarity around what a product does and where it fits helps keep the workflow predictable. For western blot workflows, the goal is often to keep the scientific rationale and the purchasing record aligned. The 180 kDa Plus Prestained Protein Marker is a prestained mixture of eleven recombinant proteins ranging from 12 kDa to 180 kDa. Three different chromophores (orange-red, blue and green) are bound to the proteins, producing a brightly colored marker. Because projects evolve, we aim for descriptions that remain searchable, specific, and easy to compare across catalog numbers—so you can reorder confidently and keep documentation consistent. For small teams, a description that is both searchable and specific can save time in procurement, training, and routine method documentation. For small teams, a description that is both searchable and specific can save time in procurement, training, and routine method documentation.\u003c\/p\u003e\u003ch2\u003eApplications \u0026amp; compatibility\u003c\/h2\u003e\u003cp\u003eApplications and compatibility depend on your assay design, sample type, and instrumentation. Based on the supplied information, it’s positioned for western blot workflows where clear documentation and straightforward compatibility notes matter. If you’re matching this item to an established SOP, use the product name, catalog number, and the supplied features as the primary reference points. If your workflow spans multiple instruments or sample types, look for the compatibility wording here to keep product selection and documentation aligned.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIdeal for:\u003c\/strong\u003e research groups running western blot workflows who value straightforward documentation, predictable fit, and product pages that stay aligned with the supplied technical details. Ideal when you need a quick, confident match between what’s on the page and what’s in your records.\u003c\/p\u003e","brand":"Vazyme Biotech","offers":[{"title":"100 RXNS","offer_id":57911528128857,"sku":"MP201-01","price":123.0,"currency_code":"EUR","in_stock":true},{"title":"500 RXNS","offer_id":57911528161625,"sku":"MP201-02","price":489.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/180-kda-plus-prestained-protein-marker.png?v=1777032528"},{"product_id":"bca-protein-quantification-kit","title":"BCA Protein Quantification Kit","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eBCA Protein Quantification Kit is a research-use kit supporting protein quantification workflows. The protein reduces Cu2+ to Cu+ under alkaline conditions. Key notes from the supplied features include: Simple operationHigh sensitivityBroad compatibilityHigh linear relationship of the standard curve. To support repeatable purchasing and recordkeeping, the copy reflects the supplied description and features—without overpromising beyond what’s provided.\u003c\/p\u003e\u003ch2\u003eKey Benefits\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eSimple operationHigh sensitivityBroad compatibilityHigh linear relationship of the standard curve.\u003c\/li\u003e\n\u003cli\u003eThe protein reduces Cu2+ to Cu+ under alkaline conditions.\u003c\/li\u003e\n\u003cli\u003eThen, Cu+ interacts with the unique BCA Reagent A (containing BCA) to preform a sensitive color reaction,forming coordination complexs.\u003c\/li\u003e\n\u003cli\u003eThe water-soluble complex has strong absorbance at A562 nm.\u003c\/li\u003e\n\u003cli\u003eIts absorbance and protein concentrationhave a good linear relationship in a wide range, and the protein concentration can be calculated according to the absorbance value.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it supports your workflow\u003c\/h2\u003e\u003cp\u003eResearch workflows move faster when the product choice, rationale, and documentation are all in sync—especially for routine assays and repeat ordering. For protein quantification workflows, the goal is often to keep the scientific rationale and the purchasing record aligned. The protein reduces Cu2+ to Cu+ under alkaline conditions. Then, Cu+ interacts with the unique BCA Reagent A (containing BCA) to preform a sensitive color reaction,forming coordination complexs. The water-soluble complex has strong absorbance at A562 nm. Because projects evolve, we aim for descriptions that remain searchable, specific, and easy to compare across catalog numbers—so you can reorder confidently and keep documentation consistent. It also helps when you need to hand off a method to a colleague, reference a catalog item in a report, or keep purchasing approvals moving without back-and-forth.\u003c\/p\u003e\u003ch2\u003eApplications \u0026amp; compatibility\u003c\/h2\u003e\u003cp\u003eCompatibility is most useful when it’s stated plainly, so teams can match products to their existing workflows. Based on the supplied information, it’s positioned for protein quantification workflows where clear documentation and straightforward compatibility notes matter. If you’re matching this item to an established SOP, use the product name, catalog number, and the supplied features as the primary reference points. Use the application notes as a scope guide: they indicate fit and compatibility language drawn from the supplied product information, not assumptions beyond it.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIdeal for:\u003c\/strong\u003e teams building or refining protein quantification workflows workflows, especially when multiple users need the same language for ordering, reporting, and day-to-day bench notes. Ideal when you need a quick, confident match between what’s on the page and what’s in your records.\u003c\/p\u003e","brand":"Vazyme Biotech","offers":[{"title":"250 RXNS","offer_id":57911532978521,"sku":"E112-01","price":86.0,"currency_code":"EUR","in_stock":true},{"title":"500 RXNS","offer_id":57911533011289,"sku":"E112-02","price":138.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/bca-protein-quantification-kit.png?v=1777032568"},{"product_id":"proteinase-k-20-mg-ml","title":"Proteinase K (20 mg\/ml)","description":"\u003ch2\u003eOverview\u003c\/h2\u003e\u003cp\u003eProteinase K is a research-use reagent supporting nucleic acid isolation workflows. The wording is kept close to the supplied product information, helping you reference the right item quickly and document consistently. It’s written for straightforward purchasing decisions and clean handoffs between team members.\u003c\/p\u003e\u003ch2\u003eKey Benefits\u003c\/h2\u003e\u003cul\u003e\n\u003cli\u003eClear, structured description for faster review and fewer purchasing errors.\u003c\/li\u003e\n\u003cli\u003eLanguage anchored to the supplied description and features to avoid unsupported claims.\u003c\/li\u003e\n\u003cli\u003eHelps keep ordering, labeling, and reporting aligned across projects.\u003c\/li\u003e\n\u003c\/ul\u003e\u003ch2\u003eHow it supports your workflow\u003c\/h2\u003e\u003cp\u003eIn day-to-day research, teams often need products that fit existing methods while remaining easy to justify in notes, SOPs, and reporting. For nucleic acid isolation workflows, the goal is often to keep the scientific rationale and the purchasing record aligned. Because projects evolve, we aim for descriptions that remain searchable, specific, and easy to compare across catalog numbers—so you can reorder confidently and keep documentation consistent. Clear product wording is particularly helpful when you are comparing alternatives, standardizing across projects, or documenting why a specific catalog number was selected. Clear product wording is particularly helpful when you are comparing alternatives, standardizing across projects, or documenting why a specific catalog number was selected. For small teams, a description that is both searchable and specific can save time in procurement, training, and routine method documentation. It also helps when you need to hand off a method to a colleague, reference a catalog item in a report, or keep purchasing approvals moving without back-and-forth. If your team maintains SOPs, spreadsheets, or ELN templates, consistent product language can reduce confusion between similarly named items and keep reorders accurate.\u003c\/p\u003e\u003ch2\u003eApplications \u0026amp; compatibility\u003c\/h2\u003e\u003cp\u003eUse the notes below to gauge fit for your setup and documentation needs. Based on the supplied information, it’s positioned for nucleic acid isolation workflows where clear documentation and straightforward compatibility notes matter. If you’re matching this item to an established SOP, use the product name, catalog number, and the supplied features as the primary reference points. Use the application notes as a scope guide: they indicate fit and compatibility language drawn from the supplied product information, not assumptions beyond it.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eIdeal for:\u003c\/strong\u003e labs focused on nucleic acid isolation workflows; teams that need clear, searchable documentation for purchasing and experimental records; and groups standardizing methods across projects or sites. Ideal when you need a quick, confident match between what’s on the page and what’s in your records.\u003c\/p\u003e","brand":"Vazyme Biotech","offers":[{"title":"1 ml","offer_id":57911533633881,"sku":"DE102-01","price":28.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/proteinase-k-20-mg-ml.png?v=1777032579"},{"product_id":"gold-protein-detection-kit-for-membranes","title":"Gold Protein Detection Kit for Membranes","description":"\u003cp\u003eIn workflows involving Western blotting, protein detection, and blotting workflows, the gold-based protein detection kit for membrane workflows format is positioned as a defined kit configuration rather than a generic listing.\u003c\/p\u003e\n\u003cp\u003eThis membrane-oriented kit uses a stabilized gold solution for detecting proteins blotted onto supported membranes such as nitrocellulose or PVDF, as stated in the product data. The gold particles accumulate on bound protein through ionic and hydrophobic interactions.\u003c\/p\u003e\n\u003cp\u003eChoose this product when the goal is membrane protein detection or blot visualization using a gold-based staining approach rather than antibody-nanoparticle conjugation. It is distinct from nanoparticle conjugation kits because its role is detection on membranes.\u003c\/p\u003e\n\u003cp\u003eThe exact kit contents and quantities remain in the separate specification fields, so this description focuses on the scientific role of the kit in the workflow and avoids turning the product text into a protocol.\u003c\/p\u003e\n\u003cp\u003eThe application profile includes Western blotting, blotting workflows, and protein detection. These terms reflect the supported scientific workflows for this listing and help scientists compare related products by use case, not by material alone.\u003c\/p\u003e\n\u003cp\u003eFor procurement teams, the kit should be matched to the chemistry and workflow step already defined by the assay plan. It should not be substituted for a standalone nanoparticle unless the kit format is specifically required.\u003c\/p\u003e\n\u003cp\u003eFor procurement and product selection, compare it with related nanoparticles by particle size, surface chemistry, formulation and listed application rather than treating all nanoparticles as interchangeable.\u003c\/p\u003e\n\u003ch3\u003eWorkflow use cases\u003c\/h3\u003e\n\u003cul\u003e\n  \u003cli\u003eWestern blotting and membrane-based protein detection\u003c\/li\u003e\n  \u003cli\u003eBlotting workflows using nanoparticle-based labels or conjugates\u003c\/li\u003e\n  \u003cli\u003eProtein detection on supported membrane formats\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"Cytodiagnostics","offers":[{"title":"Kit","offer_id":58053334139225,"sku":"SR-07-01","price":235.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/Support-Reagents-Category-Image.jpg?v=1778675968"},{"product_id":"protein-a-100nm-gold-conjugate","title":"Protein A - 100nm Gold Conjugate","description":"\u003ch2\u003eProtein A - 100nm Gold Conjugate for gold nanoparticle labelling\u003c\/h2\u003e\u003cp\u003eProtein A - 100nm Gold Conjugate supports method development where compatible immunoglobulins through Protein A binding must be detected in Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eScientific fit\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. This large-format gold label emphasizes strong particle visibility; scientists should optimize blocking, flow and wash conditions for the sample matrix.\u003c\/p\u003e\u003ch3\u003eProtocol notes\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eSupports Immunoblotting, Light Microscopy and Electron Microscopy workflows where Protein A signal needs to be interpreted with appropriate controls.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-100-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. For protocol transfer, record the catalog reference together with the selected application and control strategy.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088243560793,"sku":"AC-100-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088243593561,"sku":"AC-100-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088243626329,"sku":"AC-100-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088243659097,"sku":"AC-100-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/80nm-Gold-Conjugate_c19ab856-6b70-4ba4-af8d-e63295bca8e3.jpg?v=1779133378"},{"product_id":"protein-a-100nm-gold-nanourchins","title":"Protein A - 100nm Gold NanoUrchins","description":"\u003ch2\u003eProtein A - 100nm Gold NanoUrchins for NanoUrchin-based assays\u003c\/h2\u003e\u003cp\u003eProtein A - 100nm Gold NanoUrchins is a gold NanoUrchin conjugate for detecting compatible immunoglobulins through Protein A binding in Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eWorkflow value\u003c\/h3\u003e\u003cp\u003eIts NanoUrchin morphology supports red-shifted plasmon behavior and enhanced optical response compared with spherical particles of similar core size. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eAssay context\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. This compact gold format gives a balance of accessibility and signal, making it useful across immunoblotting and microscopy method development.\u003c\/p\u003e\u003ch3\u003eExperimental considerations\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eHelps connect Protein A recognition to Immunoblotting, Light Microscopy and Electron Microscopy while keeping the experimental purpose clear for protocol planning.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-20-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eAssay context\u003c\/h3\u003e\u003cp\u003eThe silver nanoparticle label is useful when a bright silver-based optical readout is preferred over a traditional gold readout. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eScientific fit\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. This mid-sized gold particle is a practical choice when both particle visibility and access to the labelled target must be balanced.\u003c\/p\u003e\u003ch3\u003eProtocol notes\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eSupports Immunoblotting, Light Microscopy and Electron Microscopy workflows where Protein A signal needs to be interpreted with appropriate controls.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-30-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eAssay context\u003c\/h3\u003e\u003cp\u003eThe silver nanoparticle label is useful when a bright silver-based optical readout is preferred over a traditional gold readout. This mid-sized silver format offers a practical balance between signal visibility and reagent accessibility.\u003c\/p\u003e\u003ch3\u003eExperimental considerations\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eHelps connect Protein A recognition to Immunoblotting, Light Microscopy and Electron Microscopy while keeping the experimental purpose clear for protocol planning.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference SC-30-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eWorkflow value\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eScientific fit\u003c\/h3\u003e\u003cp\u003eThe silver nanoparticle label is useful when a bright silver-based optical readout is preferred over a traditional gold readout. 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It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eHow it fits into the workflow\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. The larger gold label can improve visual contrast while still fitting many membrane, blotting and microscopy workflows.\u003c\/p\u003e\u003ch3\u003ePractical use in the lab\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eSupports Immunoblotting, Light Microscopy and Electron Microscopy workflows where Protein A signal needs to be interpreted with appropriate controls.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-50-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. Use this context to compare related conjugates by target, label family and experimental readout.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088248312153,"sku":"AC-50-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088248344921,"sku":"AC-50-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088248377689,"sku":"AC-50-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088248410457,"sku":"AC-50-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/50nm-Gold-Conjugate_fc9e9d10-23d8-462b-a908-681f151afbf8.jpg?v=1779133386"},{"product_id":"protein-a-50nm-gold-nanourchins","title":"Protein A - 50nm Gold NanoUrchins","description":"\u003ch2\u003eProtein A - 50nm Gold NanoUrchins for NanoUrchin-based assays\u003c\/h2\u003e\u003cp\u003eProtein A - 50nm Gold NanoUrchins is a gold NanoUrchin conjugate for detecting compatible immunoglobulins through Protein A binding in Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eScientific fit\u003c\/h3\u003e\u003cp\u003eIts NanoUrchin morphology supports red-shifted plasmon behavior and enhanced optical response compared with spherical particles of similar core size. This smaller NanoUrchin format is helpful when particle access and optical response both matter in compact assay geometries.\u003c\/p\u003e\u003ch3\u003eProtocol notes\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eSupports Immunoblotting, Light Microscopy and Electron Microscopy workflows where Protein A signal needs to be interpreted with appropriate controls.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference GUAC-50-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. For reproducible work, document the selected reagent, sample matrix and detection workflow alongside the catalog entry.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088248475993,"sku":"GUAC-50-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088248508761,"sku":"GUAC-50-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088248541529,"sku":"GUAC-50-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088248574297,"sku":"GUAC-50-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/50nm-Gold-NanoUrchin-Conjugate_10dc39ad-2c72-4986-b071-989fbf37b7f5.jpg?v=1779133386"},{"product_id":"protein-a-50nm-silver-conjugate","title":"Protein A - 50nm Silver Conjugate","description":"\u003ch2\u003eProtein A - 50nm Silver Conjugate for silver nanoparticle detection\u003c\/h2\u003e\u003cp\u003eUse Protein A - 50nm Silver Conjugate when your workflow needs reliable detection of compatible immunoglobulins through Protein A binding in Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eHow it fits into the workflow\u003c\/h3\u003e\u003cp\u003eThe silver nanoparticle label is useful when a bright silver-based optical readout is preferred over a traditional gold readout. This larger silver label supports stronger visual contrast in workflows where signal strength is more important than minimal particle size.\u003c\/p\u003e\u003ch3\u003ePractical use in the lab\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eHelps connect Protein A recognition to Immunoblotting, Light Microscopy and Electron Microscopy while keeping the experimental purpose clear for protocol planning.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference SC-50-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. When comparing related products, align the target biology with the label format and the readout you plan to use.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml","offer_id":58088248672601,"sku":"SC-50-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml","offer_id":58088248705369,"sku":"SC-50-05","price":265.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/60nm-silver-conjugate_2c920de6-d1cb-4238-9bb4-486e18384208.jpg?v=1779133387"},{"product_id":"protein-a-5nm-gold-conjugate","title":"Protein A - 5nm Gold Conjugate","description":"\u003ch2\u003eProtein A - 5nm Gold Conjugate for gold nanoparticle labelling\u003c\/h2\u003e\u003cp\u003eFor protocols centered on compatible immunoglobulins through Protein A binding, Protein A - 5nm Gold Conjugate provides a focused gold nanoparticle conjugate for Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eScientific fit\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. The small gold label is well suited to dense targets, fine localization work and protocols where steric access can affect signal quality.\u003c\/p\u003e\u003ch3\u003eProtocol notes\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eHelps connect Protein A recognition to Immunoblotting, Light Microscopy and Electron Microscopy while keeping the experimental purpose clear for protocol planning.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-5-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. When comparing related products, align the target biology with the label format and the readout you plan to use.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088248803673,"sku":"AC-5-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088248836441,"sku":"AC-5-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088248869209,"sku":"AC-5-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088248901977,"sku":"AC-5-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/5nm-Gold-Conjugate_098bd5c1-f7f8-41c4-916b-9d49bf924233.jpg?v=1779133387"},{"product_id":"protein-a-60nm-gold-conjugate","title":"Protein A - 60nm Gold Conjugate","description":"\u003ch2\u003eProtein A - 60nm Gold Conjugate for gold nanoparticle labelling\u003c\/h2\u003e\u003cp\u003eProtein A - 60nm Gold Conjugate gives assay developers a defined route to detect compatible immunoglobulins through Protein A binding across Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eWorkflow value\u003c\/h3\u003e\u003cp\u003eThe colloidal gold label provides a permanent, electron-dense and optically visible signal for method development and routine detection workflows. The larger gold label can improve visual contrast while still fitting many membrane, blotting and microscopy workflows.\u003c\/p\u003e\u003ch3\u003eUse-case guidance\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eFits workflows that require clear Protein A detection and a reagent choice that can be documented consistently.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference AC-60-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. When comparing related products, align the target biology with the label format and the readout you plan to use.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088248967513,"sku":"AC-60-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088249000281,"sku":"AC-60-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088249033049,"sku":"AC-60-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088249065817,"sku":"AC-60-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/50nm-Gold-Conjugate_b3e9c477-c384-43fb-9136-7c2811c4c219.jpg?v=1779133388"},{"product_id":"protein-a-60nm-gold-nanourchins","title":"Protein A - 60nm Gold NanoUrchins","description":"\u003ch2\u003eProtein A - 60nm Gold NanoUrchins for NanoUrchin-based assays\u003c\/h2\u003e\u003cp\u003eProtein A - 60nm Gold NanoUrchins supports method development where compatible immunoglobulins through Protein A binding must be detected in Immunoblotting, Light Microscopy and Electron Microscopy. It helps researchers evaluate target fit, assay readout and control strategy before selecting a related label or antibody format.\u003c\/p\u003e\u003ch3\u003eHow it fits into the workflow\u003c\/h3\u003e\u003cp\u003eIts NanoUrchin morphology supports red-shifted plasmon behavior and enhanced optical response compared with spherical particles of similar core size. This smaller NanoUrchin format is helpful when particle access and optical response both matter in compact assay geometries.\u003c\/p\u003e\u003ch3\u003ePractical use in the lab\u003c\/h3\u003e\u003cul\u003e\n\u003cli\u003eHelps connect Protein A recognition to Immunoblotting, Light Microscopy and Electron Microscopy while keeping the experimental purpose clear for protocol planning.\u003c\/li\u003e\n\u003cli\u003eUseful when the primary antibody class is compatible with Protein A binding and a species-independent detection strategy is desired.\u003c\/li\u003e\n\u003cli\u003eInclude matched negative controls and optimize blocking to separate true target-associated signal from nonspecific particle binding.\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eReference GUAC-60-05-05 in protocols, purchasing notes and internal reagent libraries when matching this product to your chosen assay. This makes the reagent easier to evaluate during assay planning, troubleshooting and method transfer.\u003c\/p\u003e","brand":"Cytodiagnostics","offers":[{"title":"0.5 ml \/ 3 OD","offer_id":58088250343769,"sku":"GUAC-60-05-05","price":145.0,"currency_code":"EUR","in_stock":true},{"title":"0.5 ml \/ 10 OD","offer_id":58088250376537,"sku":"GUAC-60-05-10","price":265.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 3 OD","offer_id":58088250409305,"sku":"GUAC-60-05","price":255.0,"currency_code":"EUR","in_stock":true},{"title":"1 ml \/ 10 OD","offer_id":58088250442073,"sku":"GUAC-60-05-15","price":465.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/50nm-Gold-NanoUrchin-Conjugate_4ed80a43-c931-4338-baf9-acb00e0c378c.jpg?v=1779133389"}],"url":"https:\/\/absource.de\/collections\/proteins.oembed?page=8","provider":"Absource Diagnostics","version":"1.0","type":"link"}