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CD42a antibody (AA 17-147)

The Mouse Monoclonal anti-CD42a antibody has been validated for FACS and ELISA. It is suitable to detect CD42a in samples from Human.
Catalog No. ABIN7193213

Quick Overview for CD42a antibody (AA 17-147) (ABIN7193213)

Target

See all CD42a (GP9) Antibodies
CD42a (GP9) (Glycoprotein IX (Platelet) (GP9))

Reactivity

  • 67
  • 12
  • 9
  • 8
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 43
  • 30
Mouse

Clonality

  • 44
  • 28
  • 1
Monoclonal

Conjugate

  • 41
  • 9
  • 6
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CD42a antibody is un-conjugated

Application

  • 37
  • 28
  • 23
  • 19
  • 17
  • 15
  • 11
  • 2
  • 2
  • 1
Flow Cytometry (FACS), ELISA

Clone

4E2G7
  • Binding Specificity

    • 14
    • 8
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 17-147

    Purpose

    CD42A Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human CD42A (AA: 17-147) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    CD42a (GP9) (Glycoprotein IX (Platelet) (GP9))

    Alternative Name

    CD42A

    Background

    This gene encodes a small membrane glycoprotein found on the surface of human platelets. It forms a 1-to-1 noncovalent complex with glycoprotein Ib, a platelet surface membrane glycoprotein complex that functions as a receptor for von Willebrand factor. The complete receptor complex includes noncovalent association of the alpha and beta subunits with the protein encoded by this gene and platelet glycoprotein V. Defects in this gene are a cause of Bernard-Soulier syndrome, also known as giant platelet disease. These patients have unusually large platelets and have a clinical bleeding tendency.

    Molecular Weight

    19 kDa

    Gene ID

    2815
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