StarGate® Acceptor Vector pDSG-IBA104
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StarGate® Acceptor Vector pDSG

-IBA104
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  • IBA Lifesciences已认证
  • 德国
  • 5-5221-001
  • 2025年12月17日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4-8/-20

    • 保质期

      12 months

    • 英文名

      StarGate® Acceptor Vector pDSG-IBA104

    • 供应商

      IBA Lifesciences

    pDSG-IBA104 is a small transient expression vector encoding an N-terminal Twin-Strep-tag® and was especially developed for the use in combination with the MEXi mammalian expression system. The vector carries an ampicillin resistance cassette for selection of transformed E. coli cells and the ColE1 replication origin (pUC) for a high plasmid copy number. In addition, it contains the human cytomegalovirus (CMV) immediate-early promoter for high-level expression and the origin of replication from Epstein-Barr Virus (oriP) for extrachromosomal replication driven by EBNA-1 expressed by MEXi-293E cells. The expressed protein is transferred into the medium due to the BM40 secretory signal peptide. During translocation from the cytosol the signal peptide is removed from the protein by endogenous proteases. Please note that cloning into pDSG-IBA acceptor vectors compulsorily requires the restriction enzyme Esp3I since no other MCS for the integration of a gene of interest is available. In addition to the direct cloning of the gene of interest into pDSG-IBA vectors with Esp3I, another option via a so-called entry vector is possible.

    Specifications

    Affinity Tag N'-terminal:Twin-Strep-tag®
    Cloning Method:Direct cloning using restriction enzyme Esp3I
    Concentration:250 ng/µl
    Expression Host:Mammalian cells, MEXi-293E cells
    Form:Suspension in TE buffer
    Possible Application:Vector for recombinant expression in mammalian cells
    Promoter:CMV Promoter
    Resistance:Ampicillin
    Sequence:See Documents
    Size:5874 bp

    Shipping information

    Storage:-20 °C
    Stability:12 months after shipping
    Shipping:Room temperature

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    图标文献和实验
    该产品被引用文献

    [1] Bochel A, Mortensen S A, Seifert L, et al. Structure of the N-terminal didomain d1_d2 of the Thrombospondin type-1 domain-containing 7A[J]. bioRxiv, 2023: 2023.05. 03.539264.

    [2] Seifert L, Zahner G, Meyer-Schwesinger C, et al. The classical pathway triggers pathogenic complement activation in membranous nephropathy[J]. Nature Communications, 2023, 14(1): 473.

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    StarGate® Acceptor Vector pDSG-IBA104
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