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Signal Transduction Protein Phosphorylation Ser / Thr Kinases Aurora

Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)

Price and availability

606 422 ₸

Availability

Order now and get it on Thursday June 01, 2023

Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
  • 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 [EPR20389] to Aurora B (phospho S227) - BSA and Azide free
  • Suitable for: Dot blot, WB, IP, ICC/IF
  • Reacts with: Human

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Overview

  • Product name

    Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free
    See all Aurora B primary antibodies
  • Description

    Rabbit monoclonal [EPR20389] to Aurora B (phospho S227) - BSA and Azide free
  • Host species

    Rabbit
  • Tested applications

    Suitable for: Dot blot, WB, IP, ICC/IFmore details
  • Species reactivity

    Reacts with: Human
  • Immunogen

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

  • General notes

    ab251522 is the carrier-free version of ab210706.

    Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.

    This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.

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

    This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.

    This product is a recombinant monoclonal antibody, which offers several advantages including:

    • - High batch-to-batch consistency and reproducibility
    • - Improved sensitivity and specificity
    • - Long-term security of supply
    • - Animal-free production
    For more information see here.

    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C. Do Not Freeze.
  • Storage buffer

    pH: 7.2
    Constituent: PBS
  • Carrier free

    Yes
  • Concentration information loading...
  • Purity

    Protein A purified
  • Clonality

    Monoclonal
  • Clone number

    EPR20389
  • Isotype

    IgG
  • Research areas

    • Cell Biology
    • Cell Cycle
    • Kinases/Phosphatases
    • Aurora
    • Epigenetics and Nuclear Signaling
    • Chromatin Modifying Enzymes
    • Phosphorylation
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • Aurora
    • Cancer
    • Cell cycle
    • Kinases/phosphatases
    • Aurora

Images

  • Western blot - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    Western blot - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    All lanes : Anti-Aurora B (phospho S227) antibody [EPR20389] (ab210706) at 1/1000 dilution

    Lane 1 : Untreated HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate
    Lane 2 : HeLa treated with 100 ng/ml nocodazole for 18 hours, whole cell lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution

    Developed using the ECL technique.

    Predicted band size: 39 kDa


    Exposure time: 3 minutes


    This data was developed using ab210706, the same antibody clone in a different buffer formulation.

    Blocking and dilution buffer: 5% NFDM/TBST.

  • Immunocytochemistry - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    Immunocytochemistry - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)

    This data was developed using ab210706, the same antibody clone in a different buffer formulation.

    Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labeling Aurora B (phospho S227) with ab210706 at 1/10000 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing midbody staining (arrow) on HeLa cell line. The nuclear counterstain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
  • Immunoprecipitation - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    Immunoprecipitation - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)

    This data was developed using ab210706, the same antibody clone in a different buffer formulation.

    Aurora B (phospho S227) was immunoprecipitated from 0.35 mg of HeLa (human epithelial cell line from cervix adenocarcinoma) treated with 100 ng/ml nocodazole for 18 hours whole cell lysate with ab210706 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab210706 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution. Lane 1: HeLa treated with 100 ng/ml nocodazole for 18 hours whole cell lysate 10μg (Input). Lane 2: ab210706 IP in HeLa treated with 100 ng/ml nocodazole for 18 hours whole cell lysate. Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab210706 in HeLa treated with 100 ng/ml nocodazole for 18 hours whole cell lysate. Blocking and dilution buffer: 5% NFDM/TBST. Exposure time: 30 seconds
  • Dot Blot - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    Dot Blot - Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)

    This data was developed using ab210706, the same antibody clone in a different buffer formulation.

    Dot blot analysis of Aurora B (phospho S227) labeled with ab210706 at 1/1000 dilution. Lane 1: Aurora B (phospho S227) peptide. Lane 2: Aurora B non-phospho peptide. Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution was used as secondary antibody. Blocking/Dilution buffer: 5% NFDM/TBST. Exposure time: 3 minutes
  • Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)
    Anti-Aurora B (phospho S227) antibody [EPR20389] - BSA and Azide free (ab251522)

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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