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gfp puromycin expression vector  (Genecopoeia)


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    Structured Review

    Genecopoeia gfp puromycin expression vector
    Gfp Puromycin Expression Vector, supplied by Genecopoeia, used in various techniques. Bioz Stars score: 97/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gfp+puromycin+expression+vector/DC-DON-SH01+expression+vector+for+restriction+enzyme+cloning/pm37096780-54-19-23
    Average 97 stars, based on 4 article reviews
    gfp puromycin expression vector - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Sequencing:

    Article Title: Generation of Rh D‐negative blood using CRISPR / Cas9
    Article Snippet: RHD ‐specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD‐Exon 2‐sgRNA‐CRISPR‐Cas9 vector. .. RHD‐exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD‐HL‐stop‐HR‐donor‐puro‐GFP vector (Figure ). ..

    Article Title: Generation of Rh D-negative blood using CRISPR/Cas9.
    Article Snippet: RHD-specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD-Exon 2-sgRNA-CRISPR-Cas9 vector. .. RHD-exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD-HL-stop-HRdonor-puro-GFP vector (Figure S1). ..

    Clone Assay:

    Article Title: Generation of Rh D‐negative blood using CRISPR / Cas9
    Article Snippet: RHD ‐specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD‐Exon 2‐sgRNA‐CRISPR‐Cas9 vector. .. RHD‐exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD‐HL‐stop‐HR‐donor‐puro‐GFP vector (Figure ). ..

    Article Title: Generation of Rh D-negative blood using CRISPR/Cas9.
    Article Snippet: RHD-specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD-Exon 2-sgRNA-CRISPR-Cas9 vector. .. RHD-exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD-HL-stop-HRdonor-puro-GFP vector (Figure S1). ..

    Expressing:

    Article Title: Generation of Rh D‐negative blood using CRISPR / Cas9
    Article Snippet: RHD ‐specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD‐Exon 2‐sgRNA‐CRISPR‐Cas9 vector. .. RHD‐exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD‐HL‐stop‐HR‐donor‐puro‐GFP vector (Figure ). ..

    Article Title: Generation of Rh D-negative blood using CRISPR/Cas9.
    Article Snippet: RHD-specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD-Exon 2-sgRNA-CRISPR-Cas9 vector. .. RHD-exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD-HL-stop-HRdonor-puro-GFP vector (Figure S1). ..

    Plasmid Preparation:

    Article Title: Generation of Rh D‐negative blood using CRISPR / Cas9
    Article Snippet: RHD ‐specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD‐Exon 2‐sgRNA‐CRISPR‐Cas9 vector. .. RHD‐exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD‐HL‐stop‐HR‐donor‐puro‐GFP vector (Figure ). ..

    Article Title: Generation of Rh D-negative blood using CRISPR/Cas9.
    Article Snippet: RHD-specific gRNA was cloned into the Cas9 expression vector (SH100, GeneCopoeia, Maryland) by replacing the original AAVS1 targeting gRNA to generate the pRHD-Exon 2-sgRNA-CRISPR-Cas9 vector. .. RHD-exon 2 left and right homologous arms, containing the sequence of the premature stop code, were cloned into the GFP/puromycin expression vector (SH200, GeneCopoeia) to produce the pRHD-HL-stop-HRdonor-puro-GFP vector (Figure S1). ..



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