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Coagulation Factor X antibody

This anti-Coagulation Factor X antibody is a Mouse Monoclonal antibody detecting Coagulation Factor X in EIA. Suitable for Human.
Catalog No. ABIN452592

Quick Overview for Coagulation Factor X antibody (ABIN452592)

Target

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

Reactivity

  • 71
  • 22
  • 19
  • 8
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 59
  • 11
  • 10
  • 7
  • 1
Mouse

Clonality

  • 72
  • 15
Monoclonal

Conjugate

  • 55
  • 7
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This Coagulation Factor X antibody is un-conjugated

Application

  • 51
  • 36
  • 28
  • 15
  • 13
  • 10
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  • 8
  • 7
  • 7
  • 5
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
Enzyme Immunoassay (EIA)

Clone

F10-1
  • Specificity

    Human Factor X.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Characteristics

    Synonyms: Stuart factor, Stuart-Prower factor

    Purification

    Affinity Chromatography on Protein G.

    Immunogen

    Human Factor X.

    Isotype

    IgG1
  • Application Notes

    ELISA.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Restrictions

    For Research Use only
  • Reconstitution

    Restore with Double distillated water to a final concentration to 1.0 mg/mL.

    Buffer

    0.01 M PBS, pH 7.2 without preservatives.

    Preservative

    Without preservative

    Storage

    -20 °C

    Storage Comment

    Store the antibody (in aliquots) at -20 °C. Avoid repeated freezing and thawing.
    Shelf life: one year from despatch.

    Expiry Date

    12 months
  • Target

    Coagulation Factor X (F10)

    Background

    Factor X 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 haemorrhagic condition of variable severity.Synonyms: Stuart factor, Stuart-Prower factor

    Gene ID

    2159

    UniProt

    P00742
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