Rabbit anti-Mouse, Human Serpinh1 Polyclonal Antibody | anti-Serpinh1 antibody

Serpinh1 Antibody, HRP conjugated

Cat. Num. AAA1493818

• Gene Names: Serpinh1; J6; Cbp1; Cbp2; gp46; Hsp47; BERF-1; Serpinh2
• Reactivity: Mouse, Human
• Applications: ELISA
• Purity: >95%, Protein G Purified
• Synonyms: Serpinh1; Polyclonal Antibody; Serpinh1 Antibody; HRP conjugated; Serpin H1; Cbp1; Hsp47; 47 kDa heat shock protein; Collagen-binding protein; Colligin; Serine protease inhibitor J6; anti-Serpinh1 antibody

• Host: Rabbit
• Reactivity: Mouse, Human
• Clonality: Polyclonal
• Isotype: IgG
• Purity/Purification: >95%, Protein G Purified
• Sequence Length: 417

• Applicable Applications for anti-Serpinh1 antibody: ELISA (EIA)
• Storage Buffer: Preservative: 0.03% Proclin 300; Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
• Conjugate: HRP
• Immunogen: Recombinant mouse Serpin H1 protein
• Preparation and Storage: Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C or -80 degree C. Avoid repeated freeze.

Related Product Information for anti-Serpinh1 antibody

Binds specifically to collagen. Could be involved as a chaperone in the biosynthetic pathway of collagen.

NCBI and Uniprot Product Information

• NCBI GI #: 161353504
• NCBI GeneID: 12406
• NCBI Accession #: NP_001104513.1
• NCBI GenBank Nucleotide #: NM_001111043.1
• UniProt Accession #: P19324; Q5U4D0
• Molecular Weight: 46,534 Da
• NCBI Official Full Name: serpin H1
• NCBI Official Synonym Full Names: serine (or cysteine) peptidase inhibitor, clade H, member 1
• NCBI Official Symbol: Serpinh1
• NCBI Official Synonym Symbols: J6; Cbp1; Cbp2; gp46; Hsp47; BERF-1; Serpinh2
• NCBI Protein Information: serpin H1
• UniProt Protein Name: Serpin H1
• Protein Family: Serpin
• UniProt Gene Name: Serpinh1
• UniProt Synonym Gene Names: Cbp1; Hsp47; Colligin
• UniProt Entry Name: SERPH_MOUSE

Uniprot Description

SERPINH1: Binds specifically to collagen. Could be involved as a chaperone in the biosynthetic pathway of collagen. Defects in SERPINH1 are the cause of osteogenesis imperfecta type 10 (OI10). A connective tissue disorder characterized by bone fragility, low bone mass, bowing of limbs due to multiple fractures, short limb dwarfism and blue sclerae. Belongs to the serpin family.

Cellular Component: cytoplasm; endoplasmic reticulum; ER-Golgi intermediate compartment; extracellular space; lipid raft

Molecular Function: collagen binding; protein binding; serine-type endopeptidase inhibitor activity; unfolded protein binding

Biological Process: collagen biosynthetic process; collagen fibril organization; protein maturation