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. 2021 Jul 1;49(13):7775–7790. doi: 10.1093/nar/gkab529

Table 1.

Comparison of dCas12a efficiency when expressed from plasmid (pC-NLS, pC-NLS-Mxi1) or integrated into the genome

Fold repression eGFP fluorescence (103 MEFL)
gENO2 gENO6 gENO2 gENO6 gNone
Integrated dCas12a-NLS 8 ± 0.7 14.9 ± 1.1 21.6 ± 3.1 11.5 ± 1.8 171.7 ± 17.3
Plasmid-based dCas12a-NLS 2.2 ± 0.1 3.5 ± 0.2 37.7 ± 2.4 23.5 ± 3.3 81.8 ± 2.6
Integrated dCas12a-NLS-Mxi1 12.6 ± 0.7 8.2 ± 0.5 13.2 ± 0.8 20.3 ± 1.3 166.5 ± 18.7
Plasmid-based dCas12a-NLS-Mxi1 4.5 ± 0.3 2.3 ± 0.2 14.1 ± 1.1 27.3 ± 4.5 63.6 ± 8.1

Fold repression of eGFP expressed as an average of values normalized by a non-targeting gRNA (gNone) for four biological replicates ± 1 standard error.