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Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)

Price and availability

526 012 ₸

Availability

Order now and get it on Wednesday March 03, 2021

Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR5026] to Aurora A - BSA and Azide free
  • Suitable for: ICC/IF, Flow Cyt, IP, WB
  • Reacts with: Mouse, Human

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Overview

  • Product name

    Anti-Aurora A antibody [EPR5026] - BSA and Azide free
    See all Aurora A primary antibodies
  • Description

    Rabbit monoclonal [EPR5026] to Aurora A - BSA and Azide free
  • Host species

    Rabbit
  • Tested applications

    Suitable for: ICC/IF, Flow Cyt, IP, WBmore details
    Unsuitable for: IHC-P
  • Species reactivity

    Reacts with: Mouse, Human
  • Immunogen

    Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.

  • General notes

    ab247643 is the carrier-free version of ab108353 This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.

    Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.

    Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with

    Ab247643 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.

    Maxpar® is a trademark of Fluidigm Canada Inc.

    Rat: We have preliminary internal testing data to indicate this antibody may not react with this species. Please contact us for more information.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C. Do Not Freeze.
  • Dissociation constant (KD)

    KD = 2.63 x 10 -10 M
    Learn more about KD
  • Storage buffer

    pH: 7.2
    Constituent: PBS
  • Carrier free

    Yes
  • Concentration information loading...
  • Purity

    Affinity purified
  • Clonality

    Monoclonal
  • Clone number

    EPR5026
  • Isotype

    IgG
  • Research areas

    • Cell Biology
    • Cell Cycle
    • Cell Division
    • Spindle
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • Aurora
    • Cancer
    • Cell cycle
    • Cell division
    • Cancer
    • Tumor biomarkers
    • Other

Images

  • Western blot - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Western blot - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    All lanes : Anti-Aurora A antibody [EPR5026] - Centrosome Marker (ab108353) at 1/1000 dilution

    Lane 1 : BXPC-3 cell lysate
    Lane 2 : LnCaP cell lysate
    Lane 3 : SKBR-3 cell lysate
    Lane 4 : HepG2 cell lysate

    Lysates/proteins at 10 µg per lane.

    Predicted band size: 46 kDa



    This data was developed using ab108353, the same antibody clone in a different buffer formulation.

  • Immunocytochemistry - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Immunocytochemistry - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)

    This data was developed using ab108353, the same antibody clone in a different buffer formulation.

    Immunofluorescent staining of HeLa cells using ab108353 at 1/100
  • Immunoprecipitation - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Immunoprecipitation - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    This data was developed using ab108353, the same antibody clone in a different buffer formulation.Lane 1: Neuro2a (Mouse neuroblastoma neuroblast) whole cell lysate, 10µg
    Lane 2:
    Neuro2a cell lysate 350µg and ab109518 2µg
    Lane 3:
    Neuro2a cell lysate, 350µg and rabbit IgG (ab172730) , 2µg Purified ab108353 immunoprecipitating Aurora A in Neuro2a cell lysates. Primary antibody was used at a 1/60 dilution (20 µg/ml). For western blotting, ab108353 at 1/500 and VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1000 dilution. Blocking and diluting buffer used: 5% NFDM/TBST.
  • Immunoprecipitation - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Immunoprecipitation - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    This data was developed using ab108353, the same antibody clone in a different buffer formulation.Lane 1: HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate 10µg
    Lane 2:
    HepG2 cell lysate 350µg and ab109518 2µg
    Lane 3:
    HepG2 cell lysate 350µg and rabbit IgG (ab172730) , 2µg

    Purified ab108353 immunoprecipitating Aurora A in Neuro2a cell lysates. Primary antibody was used at a 1/60 dilution (20 µg/ml). For western blotting, ab108353 at 1/500 and VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1000 dilution. Blocking and diluting buffer used: 5% NFDM/TBST.
  • Flow Cytometry - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Flow Cytometry - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    This data was developed using ab108353, the same antibody clone in a different buffer formulation.Overlay histogram showing HeLa cells stained with ab108353 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab108353, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1?g/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
  • Western blot - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Western blot - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Anti-Aurora A antibody [EPR5026] - Centrosome Marker (ab108353) at 1/1000 dilution + Neuro-2a cell lysate at 10 µg

    Predicted band size: 46 kDa



    This data was developed using ab108353, the same antibody clone in a different buffer formulation.

  • OI-RD Scanning - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    OI-RD Scanning - Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    This data was developed using ab108353, the same antibody clone in a different buffer formulation.Equilibrium disassociation constant (KD)
    Learn more about KD

    Click here to learn more about KD
  • Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
    Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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