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Thrombomodulin antibody (AA 297-505)

This Mouse Monoclonal antibody specifically detects Thrombomodulin in ELISA and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN7193269

Quick Overview for Thrombomodulin antibody (AA 297-505) (ABIN7193269)

Target

See all Thrombomodulin (THBD) Antibodies
Thrombomodulin (THBD)

Reactivity

  • 130
  • 39
  • 22
  • 4
  • 4
  • 2
  • 1
Human

Host

  • 77
  • 73
  • 6
  • 2
  • 2
Mouse

Clonality

  • 92
  • 67
  • 1
Monoclonal

Conjugate

  • 79
  • 21
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Thrombomodulin antibody is un-conjugated

Application

  • 102
  • 77
  • 47
  • 43
  • 29
  • 29
  • 26
  • 22
  • 21
  • 14
  • 14
  • 12
  • 12
  • 5
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA, Flow Cytometry (FACS)

Clone

2C6C3
  • Binding Specificity

    • 40
    • 15
    • 6
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 297-505

    Purpose

    CD141 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human CD141 (AA: 297-505) 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

    Thrombomodulin (THBD)

    Alternative Name

    CD141

    Background

    The protein encoded by this intronless gene is an endothelial-specific type I membrane receptor that binds thrombin. This binding results in the activation of protein C, which degrades clotting factors Va and VIIIa and reduces the amount of thrombin generated. Mutations in this gene are a cause of thromboembolic disease, also known as inherited thrombophilia.

    Molecular Weight

    60.3 kDa

    UniProt

    P07204
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