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pLVX-DsRed-Monomer-C1载体

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  • ¥750
  • 盖宁生物
  • 上海
  • GN2018
  • 2025年12月25日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      常温

    • 保质期

      三年

    • 英文名

      pLVX-DsRed-Monomer-C1

    • 库存

      现货

    • 供应商

      上海盖宁生物

    质粒类型: 慢病毒载体
    高拷贝/低拷贝: 高拷贝
    启动子: CMV
    克隆方法: 多克隆位点,限制性内切酶
    载体大小: 8753 bp
    5' 测序引物及序列: CMV-F: CGCAAATGGGCGGTAGGCGTG(Invitrogen)
    载体标签: N-DsRed-Monomer
    载体抗性: Ampicillin (氨苄青霉素)
    筛选标记: 嘌呤霉素(Puromycin)

    订购信息

    产品编号 产品名称 规格 价格
    2018 pLVX-DsRed-Monomer-C1

    5ug质粒

    ¥1000.00

    质粒图谱

    pLVX-DsRed-Monomer-C1 质粒图谱

    载体描述

    描述

    pLVX-DsRed-Monomer-C1 is an HIV-1-based, lentiviral expression vector that allows you to express your gene of interest fused to DsRed-Monomer, a monomeric mutant of the Discosoma sp. red fluorescent protein. Genes cloned into the multiple cloning site (MCS), located at the C-terminal end of the DsRed-Monomer coding sequence, are expressed as C-terminal fusions of the DsRed-Monomer protein. Expression of the fusion protein is driven by the constitutively active human cytomegalovirus immediate early promoter (PCMV IE) located just upstream of the DsRed-Monomer coding sequence. Lentiviral particles derived from the vector allow the expression of DsRed-Monomer fusion proteins in virtually any cell type, including primary cells. The unmodified vector expresses DsRed-Monomer, and may be used to produce marker virus to optimize infection protocols.

    pLVX-DsRed-Monomer-C1 contains all of the viral processing elements necessary for the production of replication-incompetent lentivirus, as well as elements to improve viral titer, transgene expression, and overall vector function. The woodchuck hepatitis virus posttranscriptional regulatory element (WPRE) promotes RNA processing events and enhances nuclear export of viral and transgene RNA (1), leading to increased viral titers from packaging cells, and enhanced expression of your gene of interest in target cells. In addition, the vector includes a Rev-response element (RRE), which further increases viral titers by enhancing the transport of unspliced viral RNA out of the nucleus (2). Finally, pLVX-DsRed- Monomer-C1 also contains a central polypurine tract (cPPT) element that increases nuclear importation of the viral genome during target cell infection, resulting in improved vector integration and more efficient transduction (3).

    In addition to lentiviral elements, pLVX-DsRed-Monomer-C1 contains a puromycin resistance gene (Puror) under the control of the murine phosphoglycerate kinase (PGK) promoter (PPGK) for the selection of stable transductants. The vector also contains a pUC origin of replication and an E. coli ampicillin resistance gene (Ampr) for propagation and selection in bacteria.

    用途

    pLVX-DsRed-Monomer-C1 constitutively expresses your gene of interest from PCMV IE when transduced into target cells. Before the vector can be transduced into cells, however, it must be transfected into 293T packaging cells with our Lenti-X™ HTX Packaging System (Cat. Nos. 631247 and 631249). This packaging system allows you to safely produce high titer, infectious, replication-incompetent, VSV-G pseudotyped lentiviral particles that can infect a wide range of cell types, including non-dividing and primary cells (4).

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    *发表【中文论文】请标注:由上海盖宁生物科技有限公司提供;

    *发表【英文论文】请标注:From Shanghai Gaining Biotechnology Co., Ltd.

    相关实验
    • Convenient Determination of Protein-Binding DNA Sequences Using Quadruple 9-Mer-Based Microarray and DsRed-Monomer Fusion Protein

      in such a way that target probes are synthesized as quadruples of all possible 9-mer combinations. Also, recombinant proteins fused with DsRed-monomer fluorescent protein are conveniently constructed. Q9-PBM confirms the well-known DNA-binding sequences of Cbf

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    pLVX-DsRed-Monomer-C1载体
    ¥750