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Coagulation Factor X antibody

This anti-Coagulation Factor X antibody is a Rabbit Polyclonal antibody detecting Coagulation Factor X in IF. Suitable for Human and Mouse.
Catalog No. ABIN6568380

Quick Overview for Coagulation Factor X antibody (ABIN6568380)

Target

See all Coagulation Factor X (F10) Antibodies
Coagulation Factor X (F10)

Reactivity

  • 69
  • 20
  • 18
  • 8
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 53
  • 12
  • 10
  • 7
  • 1
Rabbit

Clonality

  • 67
  • 15
Polyclonal

Conjugate

  • 50
  • 7
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This Coagulation Factor X antibody is un-conjugated

Application

  • 46
  • 34
  • 22
  • 12
  • 10
  • 9
  • 9
  • 9
  • 7
  • 7
  • 5
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human F10 (NP_000495.1).

    Isotype

    IgG
  • Application Notes

    IF 1:10-1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Coagulation Factor X (F10)

    Alternative Name

    F10

    Background

    This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds, the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides.

    Molecular Weight

    Observed_MW: 75kDa

    Calculated_MW: 54kDa

    Gene ID

    2159

    UniProt

    P00742
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