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Factor XIIIa Recombinant Rabbit mAb

Cat No.: RMA02900
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  • Western blot analysis of Anti-Factor XIIIa antibody(RMA02900) Gel: 6%SDS-PAGE Lysate: 20 μg Primary antibody: RMA02900(Factor XIIIa antibody)at dilution 1:1000 Secondary antibody: Goat anti rabbit IgG (SPA10002)at 1:1000 dilution

Product Name: Factor XIIIa Recombinant Rabbit mAb
Cat No.: RMA02900
Clonality: Monoclonal
Species Reactivity: Human
Tested Applications: WB, IHC, ICC/IF, FC
Recommended Dilution: WB, IHC, ICC/IF, FC
Size: 30ul 50ul 100uL
Format: Liquid
Source: Rabbit
Purification Method: Affinity Purification
Isotype: IgG
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 a
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
Synonyms: F13A
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]
Category: Primary Ab
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