C5483
Human Collagen Type I
from human skin, powder, ~95% (SDS-PAGE), suitable for cell culture
製品名
コラーゲン ヒト, Bornstein and Traub Type I, acid soluble, powder, ~95% (SDS-PAGE)
biological source
human
assay
~95% (SDS-PAGE)
form
powder
technique(s)
cell culture | stem cell: suitable
solubility
aqueous acid: ≤5 mg/mL
UniProt accession no.
storage temp.
2-8°C
Quality Level
Gene Information
human ... COL1A2(1278)
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Application
I型コラーゲンは、広範な生体材料工学研究において、in vitroで幹細胞を増殖させる骨格として利用されてきました。
Human collagen has been used:
- as a component of extracellular matrix in the chemotaxis assay of the rat adipose-derived stem cells
- in adhesion assay of the adult retinal pigmented epithelium-19 (ARPE-19) cell line
- in the glycation aggregation and adsorption studies as a model system for arthritis
General description
コラ-ゲンは構造や遺伝子が異なる多数のタイプに分類されています。シグマでは、BornsteinとTraubが提唱した命名法を使用しています。シグマのタイプ分けは一般的なコラ-ゲン分類とは異なりますのでご注意ください。
Collagen type 1 alpha 2 (COL1A2) encodes pro-alpha2 chain and is a component of heterodimer, type 1 collagen fiber. It is mapped to human chromosome 7q21.3. COL1A2 associates with COL1A1 in the ratio 1:2 and undergoes posttranslational modification to form mature type I collagen fibre.
Preparation Note
Gallop, P.M.の方法の変法に従い、ヒトの皮膚から調製されています。
Biochem/physiol Actions
Collagen type 1 alpha 2 (COL1A2) is crucial for bone formation, cartilage and blood vessels. Imbalance in COL1A2 may be the cause for dental fluorosis. Missense mutations involving glycine substitutions in the COL1A2 gene alters the collagen triple helix structure decreasing its stability and is implicated in osteogenesis imperfecta. Mutations near the splice site of COL1A2 gene results in exon skipping and is associated with Ehlers-Danlos Syndrome. An insertion or deletion polymorphism in the COL1A2 gene impairs its interaction with microRNA and modulates the bone mineral density resulting in high susceptibility to osteoporosis.
保管分類
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Structural models of osteogenesis imperfecta-associated variants in the COL1A1 gene
Mooney SD and Klein TE
Molecular and Cellular Proteomics, 1(11), 868-875 (2002)
Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway
Schwarze U, et al.
American Journal of Human Genetics, 74(5), 917-930 (2004)
Integrin activation or alpha9 expression allows retinal pigmented epithelial cell adhesion on Bruch?s membrane in wet age-related macular degeneration
Afshari FT, et al.
Brain, 133(2), 448-464 (2010)
Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta
Duy BH, et al.
Human Genomics, 10(1), 27-27 (2016)
Gene expression of collagen type I alpha 2 and its relationship with dental fluorosis.
Gastelbondo-Pastrana B, et al.
Journal of Oral Research, 7(6), 172-175 (2018)
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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