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vsv g envelope expressing vector pmd2 g  (Addgene inc)


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    Structured Review

    Addgene inc vsv g envelope expressing vector pmd2 g
    Vsv G Envelope Expressing Vector Pmd2 G, supplied by Addgene inc, used in various techniques. Bioz Stars score: 98/100, based on 14780 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pmd2+g+vsv+g+envelope+vector+pmd2+g/pMD2%2EG+(Plasmid+%2312259)/pm40412468-194-13-20
    Average 98 stars, based on 14780 article reviews
    vsv g envelope expressing vector pmd2 g - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Recombinant:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    Plasmid Preparation:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    Software:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    Variant Assay:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    RNA Sequencing:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    Chromatin Immunoprecipitation:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.

    Gene Expression:

    Article Title: Rewriting regulatory DNA to dissect and reprogram gene expression.
    Article Snippet: Generating doxycycline-inducible prime editing (PE2) cell lines We generated inducible PE2 (nCas9-MMLV) prime editing cell lines by first transducing THP-1 and Jurkat cells with a EF1ɑ-rtTAIRES-Neo plasmid (Clontech, Mountain View, CA), which expresses a reverse tetracycline transactivator (rtTA) and a neomycin resistance gene from the EF1ɑ promoter.



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