Cat#:PA-3007F;Product Name:Mouse Anti-Coagulation Factor XIII, A1 Polypeptide Antibody;Synonym:F13A1; coagulation factor XIII, A1 polypeptide; F13A; TGase; factor XIIIa; coagulation factor XIII A chain; fibrinoligase; FSF, A subunit; coagulation factor XIIIa; transglutaminase A chain; transglutaminase. Plasma; fibrin stabilizing factor, A subunit; coagulation factor XIII, A polypeptide; protein-glutamine gamma-glutamyltransferase A chain; bA525O21.1 (coagulation factor XIII, A1 polypeptide); EC 2.3.2.13;Background:Defects in F13A1 are the cause of factor XIII subunit A deficiency (FA13AD) [MIM:613225]. FA13AD is an autosomal recessive disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women.;Description:Mouse Anti-Coagulation Factor XIII, A1 Polypeptide Monoclonal Antibody;Host Species:Mouse;Species Reactivity:Human;Clone#:E980.2;Isotype:IgG1;Application:IHC;Storage:Store antibody products at 2-8°C. For long term storage, aliquot and freeze at -20°C. Avoid repeated freeze/thaw cycles;Usage:For Lab Research Use Only;
F13A1; coagulation factor XIII, A1 polypeptide; F13A; TGase; factor XIIIa; coagulation factor XIII A chain; fibrinoligase; FSF, A subunit; coagulation factor XIIIa; transglutaminase A chain; transglutaminase. Plasma; fibrin stabilizing factor, A subunit; coagulation factor XIII, A polypeptide; protein-glutamine gamma-glutamyltransferase A chain; bA525O21.1 (coagulation factor XIII, A1 polypeptide); EC 2.3.2.13
Gene Introduction:
Defects in F13A1 are the cause of factor XIII subunit A deficiency (FA13AD) [MIM:613225]. FA13AD is an autosomal recessive disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women.