Optimization of mRNA lipofection in K562 cells
. | Lipid . | Lipid:DNA ratio . | Incubation time (h) . | Efficiency (%) . | Viability (%) . |
---|---|---|---|---|---|
DNA | DMRIE-C | 3:1 | 6 | 26 | 88 |
RNA | DMRIE-C | 4:1 | 2 | 22 | 80 |
. | Lipid . | Lipid:DNA ratio . | Incubation time (h) . | Efficiency (%) . | Viability (%) . |
---|---|---|---|---|---|
DNA | DMRIE-C | 3:1 | 6 | 26 | 88 |
RNA | DMRIE-C | 4:1 | 2 | 22 | 80 |
K562 cells were lipofected using DMRIE-C as described in “Materials and methods.” Cells were analyzed 24 hours after lipofection by flow cytometric analysis for enhanced green fluorescent protein (EGFP) expression to estimate transfection efficiency (= % EGFP+ cells) as well as by ethidium bromide exclusion for cell viability. Results are the mean of 4 independent experiments each with a different in vitro–transcribed mRNA batch (standard error of the mean < 2.5%).