Phospho-Aurora A (Thr288)/Aurora B (Thr232)/Aurora C (Thr198) (Clone: CC12) rabbit mAb PE Conjugate, Clone: [AuroraABC-CC12], Rabbit, Monoclonal
Biozol Catalog Number:
ABI-12-4304
Supplier Catalog Number:
12-4304
Alternative Catalog Number:
ABI-12-4304-100TESTS
Manufacturer:
Abeomics
Host:
Rabbit
Category:
Antikörper
Application:
FACS
Species Reactivity:
Human
Immunogen:
A synthetic phospho-peptide corresponding to residues surrounding human Aurora A (Thr288)/Aurora B (Thr232)/Aurora C (Thr198)
Conjugation:
PE
Alternative Names:
Aurora kinase A/B/C, AURKA, AURKB, AURKC
Aurora kinases (serine/threonine kinases) are essential requirement for the onset and progression of mitosis. These kinases share a similar protein structure as well as kinase activity, however each kinase display distinct cellular and subcellular localization. Each Aurora member is phosphorylated at specific residues upon co-factor binding during mitosis. Aurora kinases acquire active kinase conformations due to the activation loop. The active kinase conformation is acquired upon auto-phosphorylation through an intermolecular (trans)-reaction within Aurora kinase domain. Aurora Kinase A (Aurora A) is involved in G2/M transition. AuroraA promotes centrosome maturation and mitotic spindle assembly, whereas AuroraB and AuroraC act as chromosome-passenger complex proteins. They play a crucial role in chromosomal binding to kinetochores and segregation of chromosomes. Aurora B is widely distributed in the cell, while AuroraC is expressed mainly in the meiotically-active germ cells. Aurora kinases are auto-phosphorylated into active forms at conserved threonine residues (i.e. the Thr288 (AurA), Thr232 (AurB) and Thr195 (AurC) residues). AuroraA auto-phosphorylation is initiated by several co-factors acting at different steps of mitosis. AroraB and AruroaC auto-phosphorylation are mediated by survivin and Borealin proteins.
Clonality:
Monoclonal
Clone Designation:
[AuroraABC-CC12]
Form:
Conjugated
Application Dilute:
For flow cytometric staining, the suggested use of this reagent is 5 µL per million cells or 5 µL per 100 µL of staining volume. It is recommended that the reagent be titrated for optimal performance for each application. See product image legends for add
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