{"product_id":"nefm-antibody-sc-f0695","title":"Neurofilament-M Antibody","description":"\u003ch2\u003eAbout the Target\u003c\/h2\u003e\u003cp\u003eNEFM is a target of interest in many antibody-based workflows. Neurofilaments (NFs) are intermediate filaments (IFs) that form 10-nm filaments, bridging the gap in size between actin and myosin filaments. They belong to the class III IF proteins and are composed of four subunits: NF-L, NF-M, NF-H, and α-internexin or peripherin. Phosphorylation of NF-L and NF-M head domains affects their interactions with various proteins, including 14-3-3 protein, synapsin, and brain spectrin, influencing processes like neurite outgrowth. Depending on the literature source, NEFM may also be discussed as Neurofilament-M and 160 kD Neurofilament Medium.\u003c\/p\u003e\u003cp\u003eReported cellular context includes cell projection, cytoplasm, cytoskeleton, and intermediate filament, which can matter when signal is compared across treatments or changing cell states. Following NEFM 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\u003eNEFM 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 projection, cytoplasm, and cytoskeleton, 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 projection, cytoplasm, and cytoskeleton 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 NEFM. 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 NEFM reflect biology rather than handling. When interpreting NEFM, 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 NEFM 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":57577504244057,"sku":"F0695-20UL","price":159.0,"currency_code":"EUR","in_stock":true},{"title":"100 µl","offer_id":57577504276825,"sku":"F0695-100UL","price":349.0,"currency_code":"EUR","in_stock":true},{"title":"2 × 100 µl","offer_id":57577504309593,"sku":"F0695-2X100UL","price":519.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0923\/1011\/0553\/files\/F0695-IHC1.jpg?v=1773598807","url":"https:\/\/absource.de\/products\/nefm-antibody-sc-f0695","provider":"Absource Diagnostics","version":"1.0","type":"link"}