• merck millipore,默克密理博,AB769,Anti-Collagen Type IV Antibody
  • merck millipore,默克密理博,AB769,Anti-Collagen Type IV Antibody

    产品名称:Anti-Collagen Type IV Antibody
    产品型号:AB769
    Detect Collagen Type IV using this Anti-Collagen Type IV Antibody validated for use in DB, ELISA, IC, IH.

    merck millipore,默克密理博,AB769,Anti-Collagen Type IV Antibody

  • 产品介绍
  • merck millipore,默克密理博,AB769,Anti-Collagen Type IV Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    M, B, HIHC, ELISA, ICCGtAffinity PurifiedPolyclonal Antibody
    描述
    产品目录编号 AB769
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Collagen Type IV Antibody
    产品信息
    格式 Affinity Purified
    控制
    • Positive Control: Kidney, muscle, tendon spleen tissue
      Negative Control: Neurons/glia
    演示 Affinity Purified immunoglobulin. Prior to purification the antisera was adsorbed against collagen type I, II, III, V and VI immobilized on Sepharose™ 4B. Liquid in 100 mM borate buffered saline, pH 8.2, no sodium azide.
    应用
    应用 Detect Collagen Type IV using this Anti-Collagen Type IV Antibody validated for use in DB, ELISA, IC, IH.
    主要应用
    • Immunohistochemistry
    • ELISA
    • Immunocytochemistry
    不建议的应用
    • Western Blotting
    应用说明 Dot and slot blotting: 1:100-1:500

    ELISA: 1:1000-1:4000

    Indirect immunohistochemistry (frozen sections only): 1:10-1:40

    Immunocytochemistry 1:10-1:20

    Optimal working dilutions must be determined by the end user.
    生物信息
    免疫原品种 Human and bovine placental collagen type IV
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Goat
    特异性 Recognizes Human and bovine type IV collagen as demonstrated by ELISA. Less than 10% cross reactivity with collagen types I, II, III, V, and VI. May show reactivity to type IV collagen from other species. AB769 has not been tested with other extracellular matrix proteins (e.g., laminin, fibronectin).
    品种反应性 MouseBovineHuman
    抗体类型 Polyclonal Antibody
    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
    纯化方法 Immunoaffinity purified
    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 Maintain for 1 year at 2–8°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
    包装信息
    数量 200 µg

    merck millipore,默克密理博,AB769,Anti-Collagen Type IV Antibody

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