Function
The B chain of factor XIII is not catalytically active, but is thought to stabilize the A subunits and regulate the rate of transglutaminase formation by thrombin.
Biological Context
Subcellular Location: Secreted
Disease Association: Factor XIII subunit B deficiency (FA13BD) : An autosomal recessive hematologic disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women. [The disease is caused by variants affecting the gene represented in this entry]
Product Specifications
Recombinant Human Coagulation factor XIII B chain (F13B), partial is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 260-403aa, with N-terminal 10xHis-GST-tagged and C-terminal Myc-tagged tag, molecular weight 51.5kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.
