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Anti-AURKA / Aurora-A Antibody (phospho-Thr288) IHC-plus™ LS-B1664

Note: This antibody replaces LS-C41315


Wt. Vol. Conc. Price
- 50 µl 0.21 mg/ml $395
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)

Most Popular AURKA / Aurora-A Antibodies

Anti-AURKA / Aurora-A Antibody (phospho-Thr288) IHC-plus™ LS-B1664
Rabbit Polyclonal (IgG) to Human AURKA / Aurora-A
IHC - Paraffin, Western blot
Immunohistochemistry Image
Anti-AURKA / Aurora-A Antibody (aa100-150) IHC-plus™ LS-B6517
Rabbit Polyclonal to Human AURKA / Aurora-A
Human, Mouse, Rat
IHC - Paraffin, Western blot
Immunohistochemistry Image

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


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


  • IHC - Paraffin (1:50)
  • Western blot

Specificity and Use

AURKA / Aurora-A antibody was raised against synthetic peptide from human AURKA / Aurora-A.
Modified peptide
Immunohistochemistry: LS-B1664 was validated for use in immunohistochemistry on a panel of 21 formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with the primary antibody, slides were incubated with biotinylated secondary antibody, followed by alkaline phosphatase-streptavidin and chromogen. The stained slides were evaluated by a pathologist to confirm staining specificity. The optimal working concentration for LS-B1664 was determined to be 1:50.


Phosphate-buffered solution, pH 7.2, 0.09% sodium azide, 50% glycerol.
+4°C or -20°C, Avoid repeated freezing and thawing.
For research use only.

Publications (1)

Curcumin-induced mitotic spindle defect and cell cycle arrest in human bladder cancer cells occurs partly through inhibition of aurora A. Liu HS, Ke CS, Cheng HC, Huang CY, Su CL. Molecular pharmacology. 2011 80:638-46. [PubMed:21757545]

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.


Anti-AURKA / Aurora-A antibody IHC of human testis. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody LS-B1664 dilution 1:50.


Overnight nocodazole treated Hela cells stained with purified rabbit polyclonal antibody against Thr288 phosphorylated Aurora A, followed by Alexa Fluor 488-conjugated goat anti-rabbit IgG and DAPI.

Western blot

Western blot
Panel A. Extracts from untreated Hela cells (Lane 1) or overnight nocodazole-treated Hela cells (Lane 2) were immunoprecipitated with a pan-Aurora A monoclonal antibody, resolved by electrophoresis, transferred to nitrocellulose and probed with rabbit polyclonal antibody against Thr288 phosphorylated Aurora A (LS-B1664). Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.

Western blot

Western blot
Panel B. The blot shown in Panel A was stripped and re-probed with pan-Aurora specific polyclonal antibody to verify equal loading of Aurora A in the extracts. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.

Requested From: United States
Date Requested: 10/24/2016

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