• merck millipore,默克密理博,MAB3326,Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12
  • merck millipore,默克密理博,MAB3326,Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12

    产品名称:Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12
    产品型号:MAB3326
    This Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12 is validated for use in ELISA, WB, IH(P) for the detection of Collagen Type IV.

    merck millipore,默克密理博,MAB3326,Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12

  • 产品介绍
  • merck millipore,默克密理博,MAB3326,Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HWB, ELISAMPurifiedMonoclonal Antibody
    描述
    产品目录编号 MAB3326
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12
    产品信息
    格式 Purified
    控制
    • POSITIVE CONTROL: human placental tissues.
    演示 Liquid in 0.1 M sodium phosphate buffer, pH 7.0, containing 2% protease-free bovine serum albumin.
    应用
    应用 This Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12 is validated for use in ELISA, WB, IH(P) for the detection of Collagen Type IV.
    主要应用
    • Western Blotting
    • ELISA
    应用说明 Western blot. Detects human type IV collagen from human placental tissues at 2 μg/mL, giving a band at approximately 92 kDa. Optimal working dilutions must be determined by end user.
    生物信息
    表位 7S Domain
    克隆 IV-4H12
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Mouse
    特异性 Specifically reactive with human Type IV Collagen.
    同种型 IgG1κ
    品种反应性 Human
    抗体类型 Monoclonal 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
    非反应性品种
    • Rat
    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
    销售限制 This product is not available for sale in Japan.
    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.
    • Manufactured by Daiichi Fine Chemical Co., Ltd
    储存和货运信息
    存储条件 Maintain frozen at -20°C in undiluted aliquots for up to 12 months.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,MAB3326,Anti-Collagen Type IV Antibody, 7S Domain, clone IV-4H12

上一件merck millipore产品:merck millipore,默克密理博,MAB3402,Anti-Glial Fibrillary Acidic Protein Antibody, clone GA5
下一件merck millipore产品:merck millipore,默克密理博,239779,CHES, ULTROL Grade - CAS 103-47-9 - Calbiochem



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