• merck millipore,默克密理博,MAB1763,Anti-Fibulin-3 Antibody
  • merck millipore,默克密理博,MAB1763,Anti-Fibulin-3 Antibody

    产品名称:Anti-Fibulin-3 Antibody
    产品型号:MAB1763
    This Anti-Fibulin-3 Antibody is validated for use in WB for the detection of Fibulin-3.

    merck millipore,默克密理博,MAB1763,Anti-Fibulin-3 Antibody

  • 产品介绍
  • merck millipore,默克密理博,MAB1763,Anti-Fibulin-3 Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HWBMAscitesMonoclonal Antibody
    描述
    产品目录编号 MAB1763
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Fibulin-3 Antibody
    Alternate Names
    • EFEMP1
    背景信息 Fibulin-3 is a protein that belongs to a family of extracellular proteins expressed in the basement membranes of blood vessels and the gene that encodes fibulin 3 is EFEMP1. It is a secreted protein that is present in serum, urine and tissue samples. A single mutation in FBLN3 is responsible for an autosomal dominant form of macular degeneration (Marmorstein, et al., 2002)
    产品信息
    格式 Ascites
    控制
    • Positive: ARPE-19 cell line.
    演示 Ascites containg no preservatives.
    应用
    应用 This Anti-Fibulin-3 Antibody is validated for use in WB for the detection of Fibulin-3.
    主要应用
    • Western Blotting
    应用说明 Western blot: 1:100 after immunoprecipitation
    生物信息
    免疫原品种 GST-tagged fibulin-3 fusion protein containing amino acids 107-493.
    表位 amino acids 107-493
    克隆 G3-5
    宿主 Mouse
    特异性 Clone G3-5 recognizes human fibulin-3 with a MW of 55 kDa.
    同种型 IgG1
    品种反应性 Human
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_004105.3
    • NM_001039348.1
    • NM_001039349.1
    Entrez基因汇总 This gene spans approximately 18 kb of genomic DNA and consists of 12 exons. Alternative splice patterns in the 5' UTR result in three transcript variants encoding the same extracellular matrix protein. Mutations in this gene are associated with Doyne honeycomb retinal dystrophy.
    基因符号
    • MTLV
    • EFEMP1
    • FBNL
    • MLVT
    • FBLN3
    • FLJ35535
    • DRAD
    • fibrillin-like
    • Fibulin-3
    • S1-5
    • FIBL-3
    • MGC111353
    • DHRD
    UniProt编号
    • Q12805
    UniProt汇总 SIZE: 493 amino acids; 54641 Da
    SUBCELLULAR LOCATION: Secreted.
    DISEASE: SwissProt: Q12805 # Defects in EFEMP1 are a cause of Doyne honeycomb retinal dystrophy (DHRD) [MIM:126600]; also known as malattia leventinese (MLVT OR ML). DHRD is an autosomal dominant disease characterized by yellow-white deposits known as drusen that accumulate beneath the retinal pigment epithelium.
    SIMILARITY: SwissProt: Q12805 ## Belongs to the fibulin family. & Contains 6 EGF-like 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 at -20°C for up to 12 months from date of receipt in undiluted aliquots. Avoid repeated freeze/thaw cycles.
    包装信息
    数量 100 µL

    merck millipore,默克密理博,MAB1763,Anti-Fibulin-3 Antibody

上一件merck millipore产品:merck millipore,默克密理博,HTS176M,ChemiSCREEN™ Membrane Preparation Recombinant Human S1P1 Lysophospholipid Receptor
下一件merck millipore产品:merck millipore,默克密理博,ABC842,Anti-DR6 Antibody



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