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Moldovan et al., 2024)

doi: 10.1016/j.cytogfr.2021.12.002 34 McGuireMHHerbrichSMDasariSKWuSYWangYRupaimooleRet al

Program A-013) using 0.5 E 6 cells and 10 g expression plasmid in 100 l of nucleofector buffer solution (VPH-5012, Lonza) and GFP expressing cells were isolated through fluorescent activated cell sorting and evaluated by SURVEYOR Mutation Detection Kit (706020, IDT) as well as Sanger and next-generation sequencing