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ipsc cell lines atcc acs 1004  (ATCC)


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    ATCC ipsc cell lines atcc acs 1004
    Ipsc Cell Lines Atcc Acs 1004, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ipsc+cell+lines+atcc+acs+1004/ATCC-DYP0250+Human+Induced+Pluripotent+Stem+(IPS)+Cells/us12331318-90-34-37
    Average 94 stars, based on 12 article reviews
    ipsc cell lines atcc acs 1004 - by Bioz Stars, 2026-10
    94/100 stars

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    other:

    Article Title: Non-immunogenic engineered tissue and methods of producing and using the same
    Article Snippet: Further exemplary iPSC cell lines that can be used in the present invention, include but are not limited to, the Human Episomal iPSC Line of GibcoTM (order number A18945, Thermo Fisher Scientific), or the iPSC cell lines ATCC ACS-1004, ATCC ACS-1021, ATCC ACS-1025, ATCC ACS-1027 or ATCC ACS-1030 available from ATTC.



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    ATCC ipsc line
    Establishment of Gene-Corrected and <t>Compound</t> <t>Mutation</t> <t>iPSC</t> Lines from dF/dF Patient-Derived iPSCs (A) Efficiencies in generating heterozygously (dF/CT) and homozygously (CT/CT) corrected iPSC clones from a patient- (dF/dF) derived iPSC line. (B) Immunofluorescent staining of pluripotency markers in iPSCs. Scale bar, 100 μm. (C) Expression of pluripotency genes in iPSCs. Data are presented as mean ± SEM. (D) Germlayer-specific transcript levels in EBs derived from iPSC lines. Data are presented as mean ± SEM. (E) Efficiencies in generating G551D mutation clones from a dF/CT iPSC line. (F) Percentage of clones that carry the G551D/dF heterozygous compound mutations among four heterozygous G551D clones.
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    Establishment of Gene-Corrected and Compound Mutation iPSC Lines from dF/dF Patient-Derived iPSCs (A) Efficiencies in generating heterozygously (dF/CT) and homozygously (CT/CT) corrected iPSC clones from a patient- (dF/dF) derived iPSC line. (B) Immunofluorescent staining of pluripotency markers in iPSCs. Scale bar, 100 μm. (C) Expression of pluripotency genes in iPSCs. Data are presented as mean ± SEM. (D) Germlayer-specific transcript levels in EBs derived from iPSC lines. Data are presented as mean ± SEM. (E) Efficiencies in generating G551D mutation clones from a dF/CT iPSC line. (F) Percentage of clones that carry the G551D/dF heterozygous compound mutations among four heterozygous G551D clones.

    Journal: Molecular Therapy. Nucleic Acids

    Article Title: Efficient Gene Editing at Major CFTR Mutation Loci

    doi: 10.1016/j.omtn.2019.02.006

    Figure Lengend Snippet: Establishment of Gene-Corrected and Compound Mutation iPSC Lines from dF/dF Patient-Derived iPSCs (A) Efficiencies in generating heterozygously (dF/CT) and homozygously (CT/CT) corrected iPSC clones from a patient- (dF/dF) derived iPSC line. (B) Immunofluorescent staining of pluripotency markers in iPSCs. Scale bar, 100 μm. (C) Expression of pluripotency genes in iPSCs. Data are presented as mean ± SEM. (D) Germlayer-specific transcript levels in EBs derived from iPSC lines. Data are presented as mean ± SEM. (E) Efficiencies in generating G551D mutation clones from a dF/CT iPSC line. (F) Percentage of clones that carry the G551D/dF heterozygous compound mutations among four heterozygous G551D clones.

    Article Snippet: A patient-derived iPSC line (ACS-1004, ATCC) carrying the homozygous dF mutation was used. sg06-dF, which has been validated with greater than 80% indel rates ( C), was used as the targeting gRNA.

    Techniques: Mutagenesis, Derivative Assay, Clone Assay, Staining, Expressing