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Factor VII antibody (C-Term)

The Rabbit Polyclonal anti-Factor VII antibody has been validated for WB. It is suitable to detect Factor VII in samples from Human.
Catalog No. ABIN929426

Quick Overview for Factor VII antibody (C-Term) (ABIN929426)

Target

See all Factor VII (F7) Antibodies
Factor VII (F7) (Coagulation Factor VII (F7))

Reactivity

  • 55
  • 11
  • 8
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 51
  • 12
  • 8
  • 2
  • 1
Rabbit

Clonality

  • 63
  • 11
Polyclonal

Conjugate

  • 48
  • 15
  • 4
  • 3
  • 2
  • 1
  • 1
This Factor VII antibody is un-conjugated

Application

  • 57
  • 27
  • 23
  • 18
  • 17
  • 7
  • 5
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 5
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Purification

    Purified

    Immunogen

    F7 antibody was raised in rabbit using the C terminal of F7 as the immunogen
  • Application Notes

    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    F7 Blocking Peptide, , is also available for use as a blocking control in assays to test for specificity of this F7 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Concentration

    Lot specific

    Buffer

    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.

    Handling Advice

    Avoid repeated freeze/thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • Target

    Factor VII (F7) (Coagulation Factor VII (F7))

    Alternative Name

    F7

    Background

    This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Alternative splicing of this gene results in 2 transcripts. Defects in this gene can cause coagulopathy. Synonyms: Polyclonal F7 antibody, Anti-F7 antibody, coagulation factor VII, serum prothrombin conversion accelerator antibody.

    Pathways

    Response to Growth Hormone Stimulus, Platelet-derived growth Factor Receptor Signaling
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