儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆號: PT0762R
特異性: Endogenous
基因名稱: COL2A1
蛋白名稱: Collagen Type II
別名: Collagen alpha-1;II;chain;Alpha-1 type II collagen;[Cleaved into: Collagen alpha-1;II;chain;Chondrocalcin]
Organism-1: Human
基因ID-1: 1280
SwissProt-1: P02458
背景: This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008],
儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性: Monoclonal
克隆號: PT0762R
特異性: Endogenous
基因名稱: COL2A1
蛋白名稱: Collagen Type II
別名: Collagen alpha-1;II;chain;Alpha-1 type II collagen;[Cleaved into: Collagen alpha-1;II;chain;Chondrocalcin]
Organism-1: Human
基因ID-1: 1280
SwissProt-1: P02458
背景: This gene encodes the alpha-1 chain of type II collagen, a fibrillar collagen found in cartilage and the vitreous humor of the eye. Mutations in this gene are associated with achondrogenesis, chondrodysplasia, early onset familial osteoarthritis, SED congenita, Langer-Saldino achondrogenesis, Kniest dysplasia, Stickler syndrome type I, and spondyloepimetaphyseal dysplasia Strudwick type. In addition, defects in processing chondrocalcin, a calcium binding protein that is the C-propeptide of this collagen molecule, are also associated with chondrodysplasia. There are two transcripts identified for this gene. [provided by RefSeq, Jul 2008],
細(xì)胞定位: Cytoplasmic
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