Generation of XPC-GFP and GFP-DDB2 cell lines
Corresponding Organization : Erasmus MC
Other organizations : Austrian Academy of Sciences, Comprehensive Cancer Center Vienna, Medical University of Vienna, CeMM Research Center for Molecular Medicine, AC Camargo Hospital, Institute for Basic Science, Ulsan National Institute of Science and Technology
Variable analysis
- Transfection of DLD-1 and HCT116 cells with an XPC-GFP cDNA construct
- Transfection of HCT116 cells with pLentiCRISPR-v2 carrying an sgRNA targeting the start codon of the DDB2 locus and a DNA construct of GFP flanked by 60 bp sequences homologous to the DDB2 locus
- Generation of DLD-1 and HCT116 XPC KO cells transiently expressing XPC-GFP
- Generation of GFP-DDB2 HCT116 KI cells
- Use of jetPEI® transfection reagent (Polyplus) following the producer's protocol
- Selection with puromycin and FACS for GFP-positive cells
- Negative control: Not specified
- Positive control: Not specified
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