Table 2.

Optimization of mRNA lipofection in K562 cells

LipidLipid:DNA ratioIncubation time (h)Efficiency (%)Viability (%)
DNA DMRIE-C 3:1 26 88 
RNA DMRIE-C 4:1 22 80 
LipidLipid:DNA ratioIncubation time (h)Efficiency (%)Viability (%)
DNA DMRIE-C 3:1 26 88 
RNA DMRIE-C 4:1 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%).

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