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基因美电话027-88411411
MONOCLONAL ANTIBODY
鼠单克隆抗体
F13A1 (Factor XIIIa) Mouse mAb

货号:M01529

  • 规格价格
  • 100 μL 1800
  • 50 μL 1000
货期:1-2天
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  • 应用IHC;WB
  • 反应物种Human;Mouse;Rat
  • 理论分子量79.2 kDa
  • 表观分子量79kDa
  • 免疫原Full length human recombinant protein of human F13A1 (NP_000120) produced in HEK293T cell.
  • 基因ID60327 (Rat);74145 (Mouse);2162 (Human);
  • 蛋白编码P00488
  • 同义词F13A
  • 宿主物种Mouse
  • 抗体分型IgG1
  • 纯化Affinity purification
  • 储存Store at -20℃. Avoid freeze / thaw cycles.
  • 靶点背景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.
  • 推荐稀释比WB 1:2000< br/>IHC 1:150< br/>FLOW 1:100
  • 产品形式Liquid
  • Buffer 体系PBS with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
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