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Recombinant human CD105 protei

n, C-His(bs-41201P)-100ug/500ug/20ug
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  • ¥580 - 5680
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  • bs-41201P
  • 2025年10月16日
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      100ug/500ug/20ug

    规格:100ug产品价格:¥1880.0
    规格:500ug产品价格:¥5680.0
    规格:20ug产品价格:¥580.0
    产品编号bs-41201P
    英文名称Recombinant human CD105 protein, C-His
    中文名称重组人CD105蛋白
    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; Recombinant human CD105 protein, C-His
    性状Lyophilized or Liqui
    纯化方法AC
    理论分子量61.6
    实际分子量62 kDa
    浓度>0.5 mg/ml
    储存液20mM Tris-HCl (pH8.0) with 150mM NaCl.
    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Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    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]

     

     

    产品细节图片1
    The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.

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    图标文献和实验
    相关实验
    • Mutational Analysis of the Human Protein C Gene

      The single gene for protein C is located at position q13–q14 on chromosome 2 (1 ). Two groups have described human genomic clones of protein C isolated from phage l charon libraries using cDNA for human protein C as hybridization probes

    • Methods for Producing Recombinant Human Cellular Retinaldehyde-Binding Protein

      The cellular retinaldehyde-binding protein (CRALBP) is expressed at high levels in vertebrate visual trssue, where it may serve to modulate the interaction of 11-cis -retinol with visual-cycle enzymes in the retinal pigment epithelium (RPE

    • Expression of Recombinant Cytochromes c in E. coli

      for proper folding and stability. However, significant advances in expression of recombinant cytochromes c have been made during the last decade. It has been shown that a single gene cluster, ccmA–H , is responsible for cytochrome c maturation in Escherichia

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