CD105 Rabbit pAb, PerCP-Cy5.5 conjugated(bs-4609R-PerCP-Cy5.5)-100ul

CD105 Rabbit pAb, PerCP-Cy5.5

conjugated(bs-4609R-PerCP-Cy5.5)-100ul
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  • ¥2980
  • Bioss已认证
  • bs-4609R-PerCP-Cy5.5
  • 2025年09月30日
  • 产品信息以Bioss网站为准
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      100ul

    产品编号bs-4609R-PerCP-Cy5.5
    英文名称CD105 Rabbit pAb, PerCP-Cy5.5 conjugated
    中文名称PerCP-Cy5.5标记的内皮糖蛋白抗体
    英文别名END; Endoglin; ENG; FLJ41744; HHT1; ORW; ORW1; Osler Rendu Weber syndrome 1; RP11 228B15.2; CD 105; CD105 antigen; EGLN_HUMAN; AI528660; AI662476; S-endoglin; SN6.
    产品应用IF=1:100-500, Flow-Cyt=1ug/test

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human CD105/Endoglin
    亚型IgG
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Cancer > Tumor biomarkers

    Cardiovascular > Angiogenesis > Endothelial Cell Markers

    Cardiovascular > Cardiovascular Markers > Cell Markers > Endothelial Cells

    Cardiovascular > Vasculature > Endothelium

    Immunology > Cell Type Markers > CD > Endothelial Cells

    Stem Cells > Endothelial Progenitors > Endothelial Markers

    Stem Cells > Mesenchymal Stem Cells > Surface Molecules

    亚基Homodimer that forms an heteromeric complex with the signaling receptors for transforming growth factor-beta: TGFBR1 and/or TGFBR2. It is able to bind TGF-beta 1, and 3 efficiently and TGF-beta 2 less efficiently. Interacts with TCTEX1D4. Interacts with ARRB2.
    亚细胞定位Membrane; Single-pass type I membrane protein.
    组织特异性Endoglin is restricted to endothelial cells in all tissues except bone marrow.
    功能Major glycoprotein of vascular endothelium. May play a critical role in the binding of endothelial cells to integrins and/or other RGD receptors.
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料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 to the beta1 and beta3 peptides 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. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013]

     

    应用推荐稀释比例
    {IF}{1:100-500}
    {Flow-Cyt}{1ug/test}

     

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