Comparison

Anti-Collagen 1, alpha 1 telopeptide Antibody

Item no. ABC-AN1341
Manufacturer Abcepta
Amount 100 ul
Category
Applications WB
Specific against Cat (Feline, Felis catus), Drosophila, 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
Available
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 telopeptide primary antibody from PhosphoSolutions is rabbit polyclonal
Reactivity
B, C, Dr
Calculated Molecular Weight
138911
Formulation
Antigen Affinity Purified

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ul
Available: In stock
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