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F13A1 (Human) Matched Antibody Pair

  • Catalog # : H00002162-AP52
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  • Specification
  • Product Description:
  • This antibody pair set comes with matched antibody pair to detect and quantify protein level of human F13A1.
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Standard curve using F13A1 293T overexpression lysate (non-denatured) as an analyte.

    QC Testing of H00002162-AP52
    Sandwich ELISA detection sensitivity ranging from approximately 2187x to 9x dilution of the F13A1 293T overexpression lysate (non-denatured).
  • Supplied Product:
  • Antibody pair set content:
    1. Capture antibody: mouse monoclonal anti-F13A1, IgG2a Kappa (300 ug)
    2. Detection antibody: rabbit polyclonal anti-F13A1 (50 ul)
    *Reagents are sufficient for at least 3-5 x 96 well plates using recommended protocols.
  • Storage Instruction:
  • Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.
  • Applications
  • Application Image
  • ELISA Pair (Transfected lysate)
  • Gene Information
  • Entrez GeneID:
  • 2162
  • Gene Name:
  • F13A1
  • Gene Alias:
  • F13A
  • Gene Description:
  • coagulation factor XIII, A1 polypeptide
  • Gene Summary:
  • This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq
  • Other Designations:
  • FSF, A subunit,TGase,bA525O21.1 (coagulation factor XIII, A1 polypeptide),coagulation factor XIII A1 subunit,coagulation factor XIII, A polypeptide,factor XIIIa,fibrin stabilizing factor, A subunit,fibrinoligase,protein-glutamine gamma-glutamyltransferase
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