COL1A2 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-10155
Catalog Number: E-AB-10155
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Background:
This gene encodes the pro-alpha2 chain 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 VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.
Research Area: Cancer, Signal Transduction, Stem Cells
Synonyms:
Alpha 2 collagen type I, Alpha 2 type I collagen, Alpha 2 type I procollagen, Alpha 2(I) collagen, Alpha 2(I) procollagen, Alpha-2 type I collagen, CO1A2, COL1A2, Collagen alpha 2(I) chain, Collagen alpha-2(I) chain, Collagen I alpha 2 polypeptide, Collagen of skin tendon and bone alpha 2 chain, Collagen type I alpha 2, OI4, Osteogenesis imperfecta type IV, Type I procollagen
Immunogen: Recombinant protein of human COL1A2
Swissprot: P08123
Gene Accession: BC042586
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.1 mg/mL
Dilution: IHC 1:100-1:300
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-8787/sc-8786/sc-8785/sc-28655
This gene encodes the pro-alpha2 chain 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 VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.
Research Area: Cancer, Signal Transduction, Stem Cells
Synonyms:
Alpha 2 collagen type I, Alpha 2 type I collagen, Alpha 2 type I procollagen, Alpha 2(I) collagen, Alpha 2(I) procollagen, Alpha-2 type I collagen, CO1A2, COL1A2, Collagen alpha 2(I) chain, Collagen alpha-2(I) chain, Collagen I alpha 2 polypeptide, Collagen of skin tendon and bone alpha 2 chain, Collagen type I alpha 2, OI4, Osteogenesis imperfecta type IV, Type I procollagen
Immunogen: Recombinant protein of human COL1A2
Swissprot: P08123
Gene Accession: BC042586
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.1 mg/mL
Dilution: IHC 1:100-1:300
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-8787/sc-8786/sc-8785/sc-28655
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