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span style="font-family:"color:#000000;font-size:14px;">This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene." inertia="description">
< span style="font-family:"color:#000000;font-size:14px;">This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collage, , Mouse, " inertia="keywords">
You have no items in your shopping cart. IHC-P, WB Bovine, Equine, Monkey, Sheep Canine, Human, Mouse, Rabbit, Rat Rabbit Polyclonal Unconjugated IF, IHC, WB Human, Mouse, Rabbit Rabbit Polyclonal Unconjugated ICC, IF, IHC, WB Hamster Human, Mouse, Rat Rabbit Polyclonal Unconjugated Filter by RatingCOL1A1 Antibody
Catalog Number: orb1733149
Catalog Number orb1733149 Category Antibodies Description < span style="font-family:SimHei;">< span style="font-family:"color:#000000;font-size:14px;">This gene encodes the pro-alpha1 chains of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, Caffey Disease and idiopathic osteoporosis. Reciprocal translocations between chromosomes 17 and 22, where this gene and the gene for platelet-derived growth factor beta are located, are associated with a particular type of skin tumor called dermatofibrosarcoma protuberans, resulting from unregulated expression of the growth factor. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene<span style="color:#000000;font-size:14px;">. Species/Host Mouse Clonality Monoclonal Clone Number 4C4 Tested applications IHC Reactivity Human, Mouse, Rat Isotype Mouse IgG1 Concentration 1mg/ml Dilution range IHC: 1/100-1/200 Conjugation Unconjugated MW 139 kDa Entrez 1277 Storage Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. Buffer/Preservatives Liquid in PBS containing 50% glycerol, 0.5% rAlbumin and 0.03% Proclin 300, pH 7.3. Alternative names OI1; OI2; OI3; OI4; EDSC; CAFYD; EDSARTH1; COL1A1;
Read more...Note For research use only Expiration Date 12 months from date of receipt. Collagen I antibody [orb312178]
COL1A1 antibody [orb1294293]
Collagen I/COL1A1 Antibody [orb107158]