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Anti-Collagen 1, alpha 1 propeptide Antibody

ArtNr ABC-AN1340
Hersteller Abcepta
Menge 100 ul
Kategorie
Applikationen WB
Specific against Cattle (Bovine)
Host Rabbit
Isotype IgG
Alias Alpha 1 type I collagen antibody,Alpha 2 type I collagen antibody,alpha 2 type I procollagen antibody,alpha 2(I) procollagen antibody,alpha 2(I)-collagen antibody,Alpha-1 type I collagen antibody,alpha1(I) procollagen antibody,CO1A1_HUMAN antibody,COL1A1 antibody,COL1A2 antibody,collagen alpha 1 chain type I antibody,Collagen alpha-1(I) chain antibody,collagen alpha-1(I) chain preproprotein antibody,Collagen I alpha 1 polypeptide antibody,Collagen I alpha 2 polypeptide antibody,collagen of skin tendon and bone,alpha-1 chain antibody,collagen of skin tendon and bone alpha-2 chain antibody,Collagen type I alpha 1 antibody,Collagen type I alpha 2 antibody,EDSC antibody,OI1 antibody,OI2 antibody,OI3 antibody,OI4 antibody,pro-alpha-1 collagen type 1 antibody,type I proalpha 1 antibody,type I procollagen alpha 1 chain antibody,Type I procollagen antibody
Lieferbar
Manufacturer - Category
Primary Antibodies; Cancer; Signal Transduction; Stem Cells
Manufacturer - Targets
Collagen is an extracellular matrix protein that serves as a scaffold defining the shape and mechanical properties of many tissues and organs including skin, tendon, artery walls, fibrocartilage, bone and teeth. Type 1 collagen is the most abundant protein in mammals. Collagens are synthesized with N-terminal and C-terminal propeptides that are cleaved during maturation and secretion. After cleavage of the propeptides, the most N-terminal and C-terminal remaining sequences are known as telopeptides. Mutations in the collagen 1, alpha 1 gene (COL1A1) are known to cause osteogenesis imperfecta (aka brittle bone disease) (Byers 1989). Furthermore, mutations found in the first 90 residues of the helical region of alpha 1 collagen have been implicated in the prevention or delayed removal of the procollagen N-propeptide leading to a combined osteogenesis imperfecta and Ehlers-Danlos syndrome (EDS) phenotype (Cabral et al., 2005)
Bio Background
Collagen is an extracellular matrix protein that serves as a scaffold defining the shape and mechanical properties of many tissues and organs including skin, tendon, artery walls, fibrocartilage, bone and teeth. Type 1 collagen is the most abundant protein in mammals. Collagens are synthesized with N-terminal and C-terminal propeptides that are cleaved during maturation and secretion. After cleavage of the propeptides, the most N-terminal and C-terminal remaining sequences are known as telopeptides. Mutations in the collagen 1, alpha 1 gene (COL1A1) are known to cause osteogenesis imperfecta (aka brittle bone disease) (Byers 1989). Furthermore, mutations found in the first 90 residues of the helical region of alpha 1 collagen have been implicated in the prevention or delayed removal of the procollagen N-propeptide leading to a combined osteogenesis imperfecta and Ehlers-Danlos syndrome (EDS) phenotype (Cabral et al., 2005)
Clonality
Polyclonal
Gene Name
COL1A1
Subtitle
Our Anti-Collagen 1, alpha 1 propeptide primary antibody from PhosphoSolutions is rabbit polyclonal.
Reactivity
B
Calculated Molecular Weight
138911
Formulation
Antigen Affinity Purified

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ul
Lieferbar: In stock
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