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ELISA analysis of human serum using GTX41198 Factor VII antibody [RFF-VII/1].
ELISA analysis of human serum using GTX41198 Factor VII antibody [RFF-VII/1].
ELISA analysis of human serum using GTX41198 Factor VII antibody [RFF-VII/1].

Factor VII antibody [RFF-VII/1]

GTX41198
GeneTex
ApplicationsWestern Blot, ELISA, RadioImmunoAssay
Product group Antibodies
ReactivityHuman
TargetF7
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Overview

  • Supplier
    GeneTex
  • Product Name
    Factor VII antibody [RFF-VII/1]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody recognizes Factor VII. It may be used to detect Factor VII in immunoassays in combination with clone RFF-VII/2 (GTX41194, GTX41196) as a capture reagent.
  • Application Supplier Note
    ELISA: 1/20-1/200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, RadioImmunoAssay
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    RFF-VII/1
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID2155
  • Target name
    F7
  • Target description
    coagulation factor VII
  • Target synonyms
    coagulation factor VII; coagulation factor VII (serum prothrombin conversion accelerator); eptacog alfa; FVII coagulation protein; proconvertin; SPCA
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP08709
  • Protein Name
    Coagulation factor VII
  • Scientific Description
    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. Defects in this gene can cause coagulopathy. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides. [provided by RefSeq, Aug 2015]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203