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Rabbit Anti-SERPINH1 Antibody (CSB-PA021087ESR2HU)
Supplier: CUSABIO BIOTECH CO.
47 kDa heat shock protein Antibody,Arsenic-transactivated protein 3 Antibody,AsTP3 Antibody,Cell proliferation-inducing gene 14 protein Antibody,Collagen-binding protein Antibody,Colligin Antibody,Rheumatoid arthritis-related antigen RA-A47 Antibody,SERPINH1 Antibody,CBP1 Antibody, CBP2 Antibody, HSP47 Antibody, SERPINH2 Antibody,PIG14 AntibodyMore alternative names for the antibody
47 kDa heat shock protein antibody|serine (or cysteine) proteinase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) antibody|serine (or cysteine) proteinase inhibitor, clade H (heat shock protein 47), member 2, (collagen-binding protein 2) antibody|Serine or cysteine proteinase inhibitor clade H member 1 antibody|Serine or cysteine proteinase inhibitor clade H member 2 antibody|SERPH_HUMAN antibody|Serpin H1 antibody|Serpin peptidase inhibitor clade H member 1 antibody|serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1) antibody|Serpin peptidase inhibitor, clade H, member 1 antibody|SERPINH1 antibody|SERPINH2 antibody
Anti-Hsp47 antibody (ab77609)
Anti-Hsp47 antibody (ab77609)
Recommended applications: ELISA, WB, IHC
Recommended dilution: Recommended dilution:WB:1:200-1:1000,IHC:1:50-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Serpin H1 protein (139-418AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:510850( Cow), Entrez Gene:871( Human), Entrez Gene:12406( Mouse), Entrez Gene:29345( Rat), Omim:600943( Human), SwissProt:Q2KJH6( Cow), SwissProt:P50454( Human), SwissProt:P19324( Mouse), SwissProt:P29457( Rat), Unigene:596449( Human), Unigene:22708( Mouse), Unigene:444951( Mouse), Unigene:98199( Rat)
|Protein function|| |
Binds specifically to collagen. Could be involved as a chaperone in the biosynthetic pathway of collagen.
|Involvement in disease|| |
Osteogenesis imperfecta 10 (OI10) [MIM:613848]: A form of osteogenesis imperfecta, a connective tissue disorder characterized by low bone mass, bone fragility and susceptibility to fractures after minimal trauma. Disease severity ranges from very mild forms without fractures to intrauterine fractures and perinatal lethality. Extraskeletal manifestations, which affect a variable number of patients, are dentinogenesis imperfecta, hearing loss, and blue sclerae. OI10 is an autosomal recessive form characterized by multiple bone deformities and fractures, generalized osteopenia, dentinogenesis imperfecta, and blue sclerae. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the serpin family.
|Protein cellular localization|| |
Endoplasmic reticulum lumen.
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CUSABIO BIOTECH CO.
|Product type|| |
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