• merck millipore,默克密理博,CC076,Human Collagen Type IV
  • merck millipore,默克密理博,CC076,Human Collagen Type IV

    产品名称:Human Collagen Type IV
    产品型号:CC076


    merck millipore,默克密理博,CC076,Human Collagen Type IV

  • 产品介绍
  • merck millipore,默克密理博,CC076,Human Collagen Type IV

    重要规格表

    主要应用
    CULT
    描述
    产品目录编号 CC076
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Human Collagen Type IV
    概述 Collagen type IV is the major structural element of basal membranes. Human collagen type IV is a native triple helix. Collagen was extracted from washed dissected tissue into dilute acetic acid after mild pepsin treatment. The Collagen type IV was purified by using differential salt precipitation. Purity and retention of native helical structure was controlled by SDS-PAGE and by reaction with anti-collagen type specific monoclonal antibodies. Molecular weight: 300kDa; Solubility: 10mg/mL
    产品信息
    演示 Liquid purified protein. In 100 μL of 0.5M acetic acid solution, pH 2.5. Salt-free, no preservative.
    应用
    主要应用
    • Cell Culture
    应用说明 Coating material for cell culture studies

    Formation of collagen gels

    Optimal working dilutions must be determined by end user.
    生物信息
    浓缩 1 mg/mL
    纯度 Human collagen type IV: 95% pure by SDS-PAGE.

    Human collagen types I-III, V, VI, and non-collagen proteins:<5%. Retention of native structure was confirmed by ability to form microfibrils.
    来源 Human placenta, negative for HBsAg and HIV antibodies
    品种 Human
    Entrez基因编号
    • NM_001845.4
    Entrez基因汇总 This gene encodes the major type IV alpha collagen chain of basement membranes. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter.
    基因符号
    • arresten
    • COL4A1
    • Arresten
    UniProt编号
    • P02462
    UniProt汇总 FUNCTION: SwissProt: P02462 # Type IV collagen is the major structural component of glomerular basement membranes (GBM), forming a 'chicken-wire' meshwork together with laminins, proteoglycans and entactin/nidogen. Potently inhibits endothelial cell proliferation and angiogenesis. Inhibits angiogenesis potentially via mechanisms involving cell surface proteoglycans and the alpha and beta integrins of endothelial cells.
    SIZE: 1669 amino acids; 160615 Da
    SUBUNIT: There are six type IV collagen isoforms, alpha 1(IV)- alpha 6(IV), each of which can form a triple helix structure with 2 other chains to generate type IV collagen network.
    SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix, basement membrane.
    TISSUE SPECIFICITY: Highly expressed in placenta.
    DOMAIN: SwissProt: P02462 Alpha chains of type IV collagen have a non-collagenous domain (NC1) at their C-terminus, frequent interruptions of the G- X-Y repeats in the long central triple-helical domain (which may cause flexibility in the triple helix), and a short N-terminal triple-helical 7S domain.
    PTM: Lysines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in all cases and bind carbohydrates. & Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. & Type IV collagens contain numerous cysteine residues which are involved in inter- and intramolecular disulfide bonding. 12 of these, located in the NC1 domain, are conserved in all known type IV collagens. & The trimeric structure of the NC1 domains may be stabilized by covalent bonds between Lys and Met residues.
    DISEASE: SwissProt: P02462 # Defects in COL4A1 are a cause of brain small vessel disease with hemorrhage [MIM:607595]. Brain small vessel diseases underlie 20 to 30 percent of ischemic strokes and a larger proportion of intracerebral hemorrhages. Inheritance is autosomal dominant. & Defects in COL4A1 are a cause of porencephaly type 1 [MIM:175780]; also known as encephaloclastic porencephaly. Porencephaly is a term used for any cavitation or cerebrospinal fluid-filled cyst in the brain. Porencephaly type 1 is usually unilateral and results from focal destructive lesions such as fetal vascular occlusion or birth trauma. Inheritance is autosomal dominant.
    SIMILARITY: Belongs to the type IV collagen family. & Contains 2 COL4C (collagen IV C-terminal) 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 Store at -20ºC for up to 12 months. Avoid repeated freeze/thaw cycles.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,CC076,Human Collagen Type IV

上一件merck millipore产品:merck millipore,默克密理博,434741,ETYA - CAS 1191-85-1 - Calbiochem
下一件merck millipore产品:merck millipore,默克密理博,ABC288,Anti-SIGMAR1 Antibody



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