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prrl ws1 6 wasp  (Addgene inc)


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    Structured Review

    Addgene inc prrl ws1 6 wasp
    Prrl Ws1 6 Wasp, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/prrl+ws1+6+wasp/pRRL+WS1%2E6+WASp+(Plasmid+%2336250)/pmc12575061__10-1055-a-2508-0983-s24070322-19-61-62
    Average 93 stars, based on 1 article reviews
    prrl ws1 6 wasp - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x10 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-NucleofectorTM X Kit, program CA-137.

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region21. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)39(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch40, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x106 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-Nucleofector™ X Kit, program CA-137.

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..

    Amplification:

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x10 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-NucleofectorTM X Kit, program CA-137.

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region21. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)39(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch40, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x106 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-Nucleofector™ X Kit, program CA-137.

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..

    Clone Assay:

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x10 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-NucleofectorTM X Kit, program CA-137.

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region21. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)39(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch40, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x106 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-Nucleofector™ X Kit, program CA-137.

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..

    Bioprocessing:

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x10 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-NucleofectorTM X Kit, program CA-137.

    Article Title: Gene correction of Wiskott-Aldrich-syndrome iPS cells rescues proplatelet defects and improves platelet size.
    Article Snippet: AAVS1 gene targeting design For targeting WASP expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region21. .. For donor vector construction, the MNDWASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250)39(gifts from David Rawlings), respectively and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch40, Addgene plasmid # 22212) after removal of the CAGGS-EGFP. .. A list of primers is shown in Supplementary Table 2. iPSC gene correction 1x106 iPSCs were nucleofected with 5 ug of each nuclease vector and 10 ug of donor vector using the P3 Primary Cell 4D-Nucleofector™ X Kit, program CA-137.

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..

    Expressing:

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..

    Introduce:

    Article Title: Gene Correction of Wiskott–Aldrich syndrome iPS Cells Rescues Proplatelet Defects and Improves Platelet Size
    Article Snippet: For WASQ19X gene correction using the CRISPR/Cas9 system, 20-bp sgRNA targeting 3-nt upstream of themutation sitewas designed and cloned into the pSpCas9 (BB)-2A-GFP (px458; a gift fromFeng Zhang, Addgene plasmid # 48138).40 A 90-bp ssODN with a silence mutation at positions 15 and 18 of the gRNA-binding site was used as a template for homologous recombination (HR). .. AAVS1 Gene Targeting Design For targeting theWiskott–Aldrich syndrome protein (WASP) expression cassette at the AAVS1 site, hAAVS1L TALEN (Addgene plasmid # 35431) and hAAVS1R TALEN (Addgene plasmid # 35432), gifts from Feng Zhang, were used to introduce DNA DSB at the target region.21 For donor vector construction, the MND-WASP and the WAS1.6-WASP were amplified from pRRL-MND-WASp (Addgene plasmid # 36248) and pRRL-WS1.6-WASp (Addgene plasmid # 36250;23 gifts fromDavid Rawlings), respectively, and cloned into the AAV-CAGGS-EGFP (a gift from Rudolf Jaenisch,41 Addgene plasmid # 22212) after removal of the CAGGS-EGFP. ..



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    Addgene inc prrl ws1 6 wasp
    Prrl Ws1 6 Wasp, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/prrl+ws1+6+wasp/pRRL+WS1%2E6+WASp+(Plasmid+%2336250)/pmc12575061__10-1055-a-2508-0983-s24070322-19-61-62
    Average 93 stars, based on 1 article reviews
    prrl ws1 6 wasp - by Bioz Stars, 2026-10
    93/100 stars
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