SERPINH1 Polyclonal Antibody
|Synonyms||47 kDa heat shock protein,47 kDa heat shock protein precursor,Arsenic transactivated protein 3,Arsenic-transactivated protein 3,AsTP 3,AsTP3,CBP 1,CBP 2,CBP1,CBP2,Cell proliferation-inducing gene 14 protein,Collagen binding protein 1,Collagen binding protein 2,Collagen binding protein,Collagen-binding protein 2,Collagen-binding protein,Colligen,Colligin 1,Colligin 2,Colligin,colligin-1,colligin-2,gp46,Heat shock protein 47,Heat-shock protein 47,HGNC 1547,Hsp 47,J6,OI10,PIG 14,PIG14,PPROM,Proliferation inducing gene 14,Proliferation inducing gene 14 protein,RA A47,RA-A47,Rheumatoid arthritis antigen A 47,rheumatoid arthritis antigen A-47,Rheumatoid arthritis related antigen RA A47,Rheumatoid arthritis-related antigen RA-A47,serine (or cysteine) proteinase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1),serine (or cysteine) proteinase inhibitor, clade H (heat shock protein 47), member 2, (collagen-binding protein 2),Serine or cysteine proteinase inhibitor clade H member 1,Serine or cysteine proteinase inhibitor clade H member 2,SERPH,Serpin H1,Serpin peptidase inhibitor clade H member 1,serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1),Serpin peptidase inhibitor, clade H, member 1,SERPINH1,SERPINH2|
|Immunogen||Recombinant protein of human SERPINH1|
|Recommended dilution||WB 1:500 - 1:2000 IHC 1:50 - 1:200|
|Storage instructions||Store at -20℃. Avoid freeze / thaw cycles. |
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
|Background||This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The encoded protein is localized to the endoplasmic reticulum and plays a role in collagen biosynthesis as a collagen-specific molecular chaperone. Autoantibodies to the encoded protein have been found in patients with rheumatoid arthritis. Expression of this gene may be a marker for cancer, and nucleotide polymorphisms in this gene may be associated with preterm birth caused by preterm premature rupture of membranes. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9.|