Recombinant Human F13A (C-6His)

Recombinant Human F13A (C-6His)

规格:10µg      价格:¥760
规格:50µg      价格:¥2280
规格:500µg    价格:¥9500
SKU: PHH0612 Category: 靶点蛋白 Tags: , ,

说明书 复制

产品名称

Recombinant Human F13A (C-6His)

英文名称

Coagulation Factor XIII A Chain/F13a  

纯度

Greater than 95% as determined by reducing SDS-PAGE

内毒素

<1 EU/µg as determined by LAL test.

蛋白构建

Recombinant Human Coagulation Factor XIII A Chain is produced by our Mammalian expression system and the target gene encoding Gly39-Met732 is expressed with a 6His tag at the C-terminus.

Accession

AAH27963.1

表达宿主

Human Cells

种属

Human

预测分子量

80.3 KDa

制剂

Supplied as a 0.2 μm filtered solution of 20 mM Tris-HCl, 5% Sucrose, 10% Glycerol, 0.02% Tween 80, pH8.0.

运输方式

The product is shipped on dry ice/polar packs.Upon receipt, store it immediately at the temperature listed below.

稳定性&储存

Store at ≤ -70℃, stable for 6 months after receipt.Store at ≤ -70℃, stable for 3 months under sterile conditions after opening. Please minimize freeze-thaw cycles.

复溶

 

分子别名
Coagulation Factor XIII A Chain; Coagulation Factor XIIIa; Protein-Glutamine Gamma-Glutamyltransferase A Chain; Transglutaminase A Chain; F13A1; F13A

 

背景介绍
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.

 

注意事项

本司产品仅用于科研,不用于临床诊断和治疗

 


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