Astana Biomed Group, an authorized Abcam distributor in Central Asia

Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)

Key features and details

  • Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
  • Rabbit monoclonal [EPR7150] to Oncostatin M/OSM - BSA and Azide free
  • Suitable for: WB
  • Reacts with: Human

Overview

  • Product name

    Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free
    See all Oncostatin M/OSM primary antibodies

  • Description

    Rabbit monoclonal [EPR7150] to Oncostatin M/OSM - BSA and Azide free

  • Host species

    Rabbit

  • Tested Applications & Species

    Application Species
    WB
    Human
    See all applications and species data

  • Immunogen

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

  • Positive control

    • Jurkat, HuT-78 cell lysate; Human fetal lung tissue lysate; Human Oncostatin M recombinant protein

  • General notes

    Ab206992 is the carrier-free version of ab133748. 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

    ab206992 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.

    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

Images

  • Western blot - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    Western blot - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    All lanes : Anti-Oncostatin M/OSM antibody [EPR7150] (ab133748) at 1/1000 dilution

    Lane 1 : Jurkat cell lysate at 10 µg
    Lane 2 : Human fetal lung tissue lysate
    Lane 3 : HuT-78 cell lysate at 10 µg

    Secondary
    All lanes : Goat anti-Rabbit HRP at 1/2000 dilution

    Predicted band size: 28 kDa
    Observed band size: 22 kDa
    why is the actual band size different from the predicted?



    This data was developed using ab133748, the same antibody clone in a different buffer formulation.

  • Western blot - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    Western blot - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    Anti-Oncostatin M/OSM antibody [EPR7150] (ab133748) at 1/1000 dilution + Human Oncostatin M/OSM recombinant protein at 0.005 µg

    Secondary
    Goat anti-Rabbit HRP at 1/2000 dilution

    Predicted band size: 28 kDa
    Observed band size: 26 kDa why is the actual band size different from the predicted?



    This data was developed using ab133748, the same antibody clone in a different buffer formulation.

    Human Oncostatin M/OSM recombinant protein has a predicted MWt of 26 kDa.

  • OI-RD Scanning - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    OI-RD Scanning - Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    This data was developed using ab133748, 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-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)
    Anti-Oncostatin M/OSM antibody [EPR7150] - BSA and Azide free (ab206992)

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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