Transfection protocol of adherent HepG2 cells (96-well plate) 

1. Preparation: Cells are seeded in plates at 0.3×106cells/mL and cultured with 5%CO2 at 37℃ for 18-24h before transfection.
2. Preparation of transfection mixture:
(1). Dilute 0.5μg DNA into without DMEM medium serum(25μL in total) and homogenize gently.
(2). Dilute 0.75μL Sinofection into DMEM medium without serum(25μL in total) and homogenize gently and incubate at room temperature for 5 min.
(3). Mix the DNA and Sinofection at room temperature for 15~20min.
3. Remove the culture medium and add 50μL mixture per well.
4. After 4-6hours, remove the transfection mixture and add DMEM medium with 10%FBS.
5. Gene expression is tested after incubation with 5% CO2 at 37℃ for 48-72h.

Fig. 1 Adherent cells' Transfection

Recommended browse
Sinofection Transfection Reagent
Other cell lines
293H 293FT 293E 293F COS7 hela Caco2 BHK21 CHO-DG44 RAW264.7 MCF7 SW480 MDCK CHO-K1 A549 NIH/3T3 vero sf9
Appendix: Microscopy comparison of HepG2 cells transfected with L2K and Sinofection respectively



PDF download