Product Browser

Last updated: 2016/11/27
  • Related Product Showcase
  • By Kit

Product Compare

Product Compare Cancel Click this icon to add products to compare list. Select up to 10 products.

Quick Order (Tutorial)

Input Catalog #,
place order here!
Catalog # :
  • Where to buy
  • Choose your location

F7 (Human) ELISA Kit

  • Catalog # : KA1837
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • F7 (Human) ELISA Kit is a sandwich enzyme immunoassay for the quantitative measurement of human F7.
  • Calibration Range:
  • 0.352 to 90 ng/mL
  • Limit of Detection:
  • 0.14 ng/mL
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Standard Curve

    QC Testing of KA1837
    The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.
  • Storage Instruction:
  • Store components of the kit at 4°C or -20°C as described in the protocol.
  • Suitable Sample:
  • Cell Culture Supernatant, Plasma, Serum
  • Sample Volume:
  • 50 uL
  • Label:
  • Biotin-conjugate
  • Detection Method:
  • Colorimetric
  • Regulation Status:
  • For research use only (RUO)
  • Applications
  • Quantification
  • Application Image
  • Quantification
  • Gene Information
  • Entrez GeneID:
  • 2155
  • Gene Name:
  • F7
  • Gene Alias:
  • -
  • Gene Description:
  • coagulation factor VII (serum prothrombin conversion accelerator)
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • FVII coagulation protein,OTTHUMP00000018733,OTTHUMP00000018734,coagulation factor VII,eptacog alfa
  • Interactome
  • Interactome
  • Related Disease
  • RSS
  • YouTube
  • Linkedin
  • Facebook