Phospho-Aurora A/B/C (T288/232/198) Antibody
Selleck Chemicals
SKU:F0241-20UL
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About the Target
Phospho-Aurora A/B/C (T288/232/198) is a target of interest in many antibody-based workflows. Aurora kinases are a novel family of serine/threonine kinases that play crucial roles in regulating mitotic cell division. The family comprises three closely related members: Aurora-A, Aurora-B, and Aurora-C, which are homologs of the yeast Ipll and Drosophila aurora kinases known for their involvement in centrosome function, bipolar spindle assembly, and chromosome segregation. Depending on the literature source, Phospho-Aurora A/B/C (T288/232/198) may also be discussed as Phospho-Aurora A/B/C (T288/232/198) and Phospho Aurora A (Thr 288).
Reported cellular context includes centromere, chromosome, cytoplasm, and cytoskeleton, which can matter when signal is compared across treatments or changing cell states. Following Phospho-Aurora A/B/C (T288/232/198) across matched perturbations can help separate abundance effects from shifts in localization, complex assembly, or pathway state. In practice, this target is often considered at the family or isoform-group level, so experimental interpretation benefits from matched controls and clear comparison logic.
Research Context
Phospho-Aurora A/B/C (T288/232/198) is commonly interpreted in the context of cell cycle research, and readouts are often stronger when a study separates expression changes from compartment-level redistribution. When reported signal spans centromere, chromosome, and cytoplasm, a defined reference condition can make comparisons more interpretable across perturbations, passages, or replicate sets.
Consider these angles when interpreting target-level changes:
- apparent redistribution between centromere, chromosome, and cytoplasm across matched conditions
- cell-cycle linked differences in abundance, timing, or compartmental enrichment
- differences between total target abundance and site-specific regulation when modified forms are compared
- co-patterning with orthogonal markers and control conditions that clarify pathway state
Variant Considerations
If your project spans exploratory questions, the regular version offers a balanced option for establishing baseline signal behavior for Phospho-Aurora A/B/C (T288/232/198). This can help when protocols evolve over time and the goal is to compare experiments using a stable reference workflow.
Standardize sampling time, control choice, and downstream analysis thresholds so apparent differences in Phospho-Aurora A/B/C (T288/232/198) reflect biology rather than handling. When interpreting Phospho-Aurora A/B/C (T288/232/198), it is often useful to decide early whether the main question is overall abundance, compartmental enrichment, or context-dependent redistribution.
For multi-run studies, a shared reference condition can keep Phospho-Aurora A/B/C (T288/232/198) 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.
- Targets:
- AURKA • AURKB • AURKC
- Research Area:
- Cell Cycle
- Application:
- FCM • IF • WB
- Reactivity:
- Human • Mouse • Rat
- Specificity:
- Phospho-Aurora A/B/C (T288/232/198) Antibody [H12A24] detects endogenous levels of Aurora A/B/C only when phosphorylated at either Thr288, Thr232 or Thr198 respectively.
- Host:
- Rabbit
- Clonality:
- Monoclonal
- Clone:
- H12A24
- Storage Buffer:
- PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN₃
- Storage Temperature:
- -20°C
For Research Use Only. Not intended for diagnostic or therapeutic use.
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