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Insertion of a FLAG-tag sequence at the end of exon 9 of the TBX5 gene in three induced pluripotent stem cell lines (DHMi004-A-4, DHMi004-A-5, DHMi004-A-6) by CRISPR/Cas9 technology

Cell Research . 2024-02; 
Harald Lahm, Niraj K Singh, Irina Gottmann, Stefanie A Doppler, Elda Dzilic, Heike Preisler, Stephanie Schneider, Rüdiger Lange, Markus Krane, Martina Dreßen
Products/Services Used Details Operation
Plasmid DNA Preparation The Human Stem Cell Nucleofector Kit-1 (Lonza, Cologne) was employed to electroporate one million iPSCs with 1 μg pUC57-5′HA-TBX5-Exon9-FLAG-3′HA (GenScript, Piscataway Township, NJ) and 1 μg pX458- huTBX5-Ex9-sgRNA3 (Addgene, Watertown, MA) (Supplementary Figs. S1 and S2).  Get A Quote

摘要

The identification of TBX5-related regulatory sequences in genes essential for heart development is hampered by the absence of antibodies which allow precipitation of TBX5:DNA complexes. Employing CRISPR/Cas9 technology, we have inserted a FLAG-tag sequence at the end of exon 9 of the TBX5 gene prior to the stop codon by homologous recombination. The translated TBX5-FLAG fusion protein of the three iPSC lines can effectively be precipitated by anti-FLAG antibodies and, thus, allow the detection of specific TBX5-binding sites and their associated genes.

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