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merck millipore,默克密理博,MAB1944,Anti-Collagen Type VI Antibody, clone 3C4
产品名称:Anti-Collagen Type VI Antibody, clone 3C4
产品型号:MAB1944
This Anti-Collagen Type VI Antibody, clone 3C4 is validated for use in IC, IH for the detection of Collagen Type VI.
merck millipore,默克密理博,MAB1944,Anti-Collagen Type VI Antibody, clone 3C4
- 产品介绍
重要规格表
品种反应性 主要应用 宿主 格式 抗体类型 H IHC, ICC M Ascites Monoclonal Antibody 描述 产品目录编号 MAB1944 品牌系列 Chemicon®
商名 - Chemicon
描述 Anti-Collagen Type VI Antibody, clone 3C4 产品信息 格式 Ascites 演示 Liquid 应用 应用 This Anti-Collagen Type VI Antibody, clone 3C4 is validated for use in IC, IH for the detection of Collagen Type VI. 主要应用 - Immunohistochemistry
- Immunocytochemistry
应用说明 Immunohistochemistry (see reference). Optimal working dilutions must be determined by end user. 生物信息 免疫原品种 Purified human collagen VI 克隆 3C4 宿主 Mouse 特异性 Reacts with human collagen VI (other species not tested). 同种型 IgG1 品种反应性 Human 抗体类型 Monoclonal Antibody Entrez基因编号 - NM_001848.2
Entrez基因汇总 The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy. 基因符号 - OPLL
- COL6A1
UniProt编号 - P12109
UniProt汇总 FUNCTION: SwissProt: P12109 # Collagen VI acts as a cell-binding protein.
SIZE: 1028 amino acids; 108529 Da
SUBUNIT: Trimers composed of three different chains: alpha 1(VI), alpha 2(VI), and alpha 3(VI).
SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix (By similarity).
PTM: Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.
DISEASE: SwissProt: P12109 # Defects in COL6A1 are a cause of Bethlem myopathy (BM) [MIM:158810]. BM is a rare autosomal dominant proximal myopathy characterized by early childhood onset (complete penetrance by the age of 5) and joint contractures most frequently affecting the elbows and ankles.
SIMILARITY: SwissProt: P12109 ## Contains 3 VWFA domains.产品使用声明 使用声明 - Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
储存和货运信息 存储条件 Maintain frozen at -20°C. Avoid repeated freeze/thaw cycles. 包装信息 数量 100 µL
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