Transduction Efficiency and Peak Fluorescence Ratio of Different Cell Lines Transduced With PA317/EGFP1 Retroviral Vectors
All transductions were made by seeding 4 × 104 cells on 1.6-cm culture dishes for 24 hours and then incubating them with 100 μL of vector-containing supernatant and 4 μg/mL protamine sulphate for 48 hours more.
The ratio obtained by dividing the peak fluorescence channel of the transduced cells by the control cell peak channel.
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