F13A Protein, Human, Recombinant (His)
Ref. TM-TMPJ-00535
1mg | 2.126,00 € | ||
10µg | 135,00 € | ||
50µg | 392,00 € | ||
500µg | 1.546,00 € |
Informations sur le produit
- F13A1, Coagulation Factor XIII A Chain, Transglutaminase A Chain, F13A, Protein-Glutamine Gamma-Glutamyltransferase A Chain, Coagulation Factor XIIIa, Protein-Glutamine γ-Glutamyltransferase A Chain
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 composed of just 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. 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.
Propriétés chimiques
Question d’ordre technique sur : TM-TMPJ-00535 F13A Protein, Human, Recombinant (His)
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