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Anti-AURKA / Aurora-A Antibody (N-Terminus) LS-C41212

Catalog Size Price
LS-C41212-50 50 µl (0.49 mg/ml) Unavailable

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100% Guaranteed Publications (1)
Rabbit Polyclonal (IgG) to Mouse AURKA / Aurora-A
Mouse, Human
Immunofluorescence, Western blot


Mouse AURKA / Aurora-A
Mouse, Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Immunoaffinity purified


  • Immunofluorescence
  • Western blot

Specificity and Use

Recombinant mouse AURKA / Aurora-A.
Recombinant (partial), N-terminal


Phosphate-buffered solution, pH 7.2, 0.09% sodium azide, 50% glycerol.
Store at -20°C. Aliquot to avoid freeze/thaw cycles.
For research use only.

Publications (1)

Specialized roles of the two mitotic cyclins in somatic cells: cyclin A as an activator of M phase-promoting factor. Fung TK, Ma HT, Poon RY. Molecular biology of the cell. 2007 18:1861-73. [PubMed:17344473] [PMC:PMC1855023]

About AURKA / Aurora-A

O14965 NM_003600 NP_003591.2

AURKA Antibody, AIK Antibody, AIRK1 Antibody, ARK1 Antibody, Aurora-A kinase Antibody, Aurora kinase A Antibody, Aurora/IPL1-like kinase Antibody, AYK1 Antibody, AURA Antibody, AURORA2 Antibody, Breast tumor-amplified kinase Antibody, Breast-tumor-amplified kinase Antibody, BTAK Antibody, HARK1 Antibody, IPL1-related kinase Antibody, Serine/threonine kinase 6 Antibody, STK7 Antibody, STK6 Antibody, PPP1R47 Antibody, ARK-1 Antibody, Aurora 2 Antibody, Aurora-A Antibody, Aurora-related kinase 1 Antibody, Aurora/IPL1-related kinase 1 Antibody, IAK1 Antibody, Serine/threonine kinase 15 Antibody, STK15 Antibody

Mitotic serine/threonine kinases that contributes to the regulation of cell cycle progression. Associates with the centrosome and the spindle microtubules during mitosis and plays a critical role in various mitotic events including the establishment of mitotic spindle, centrosome duplication, centrosome separation as well as maturation, chromosomal alignment, spindle assembly checkpoint, and cytokinesis. Required for initial activation of CDK1 at centrosomes.


Overnight nocodazole treated Hela cells stained with purified rabbit polyclonal antibody against Aurora A, followed by Rhodamine Red-X conjugated goat anti-rabbit IgG and DAPI.

Western blot

Western blot
Hela cell nuclear extract was resolved by electrophoresis, transferred to nitrocellulose, and probed with rabbit anti-Aurora A antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.

Requested From: 
Date Requested: 3/21/2018

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