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Endoglin 抗体

ENG 适用: 人 FACS, IHC, ELISA, ICC 宿主: 小鼠 Monoclonal 3A9 unconjugated
产品编号 ABIN969012
发货至: 中国
  • 抗原 See all Endoglin (ENG) 抗体
    Endoglin (ENG)
    适用
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    宿主
    • 108
    • 84
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    小鼠
    克隆类型
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    单克隆
    标记
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    This Endoglin antibody is un-conjugated
    应用范围
    • 142
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    Flow Cytometry (FACS), Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC)
    原理
    CD105 Antibody
    纯化方法
    Ascitic fluid
    免疫原
    Purified recombinant fragment of human CD105 expressed in E. Coli.
    克隆位点
    3A9
    亚型
    IgG1
    Top Product
    Discover our top product ENG Primary Antibody
  • 应用备注

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Ascitic fluid containing 0.03 % sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Valeria, Maddalena, Enrica, Onofrio, Gaetano: "Endoglin (CD105) expression in the human heart throughout gestation: an immunohistochemical study." in: Reproductive sciences (Thousand Oaks, Calif.), Vol. 15, Issue 10, pp. 1018-26, (2008) (PubMed).

    Fujita, Ewing, Chan, Mangold, Partin, Isaacs, Pavlovich: "Endoglin (CD105) as a urinary and serum marker of prostate cancer." in: International journal of cancer. Journal international du cancer, Vol. 124, Issue 3, pp. 664-9, (2008) (PubMed).

  • 抗原
    Endoglin (ENG)
    别名
    CD105 (ENG 产品)
    别名
    ENG antibody, MGC137842 antibody, DKFZp469D0419 antibody, END antibody, HHT1 antibody, ORW1 antibody, AI528660 antibody, AI662476 antibody, CD105 antibody, S-endoglin antibody, endoglin antibody, ENG antibody, Eng antibody
    背景

    Description: This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds TGFB1 and TGFB3 with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia.

    Aliases: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744

    分子量
    71kDa
    基因ID
    2022
    HGNC
    2022
    UniProt
    P17813
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