Factor XIIIa Recombinant Rabbit mAb
Cat No.: ARM2899
Size：
| Product Name: | Factor XIIIa Recombinant Rabbit mAb |
| Cat No.: | ARM2899 |
| source: | Rabbit |
| reactivity: | Human |
| applications: | WB, IHC, ICC/IF, FC |
| clonality: | Monoclonal |
| recommended dilution: | WB, IHC, ICC/IF, FC |
| format: | Liquid |
| isotype: | IgG |
| immunogen: | Recombinant protein of human Factor XIIIa |
| calculated molecular weight: | 83 kDa |
| observed molecular weight: | 83 kDa |
| genbank accession number: | P00488 |
| gene id (ncbi): | 2162 |
| purification method: | Affinity Purification |
| conjugate: | Un-conjugated |
| storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt. |
| synonyms: | F13A |
| category: | Primary Ab |
| concentration: | 1mg/ml |
| background: | 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, Jul 2008] |