STEPS:
- One day before transfecting, seed cells (in a well plate) so that they are 70-90% confluent at time of transfection.
- Dilute Lipofectamine LTX Reagent in Opti-MEM Medium (Ratio =
- Dilute DNA in Opti-MEM Medium, then add PLUS Reagent (Ratio = 50uL Opti-MEM: 1ug DNA: 1uL PLUS).
- Add diluted DNA to diluted Lipofectamine LTX Reagent in a 1:1 ratio.
- Incubate at room temperature for 5 minutes.
- Add DNA-lipid complex to cells.
- Incubate cells for 1-3 days at 37C.
- Visualize/analyze transfected cells (flow cytometry).
n-WELL PLATE PROPORTIONS:
STEP | COMPONENT | 6-well | 24-well | 96-well |
---|---|---|---|---|
1. | Adherent Cells | 0.25-1 x 10^6 | 0.5-2 x 10^5 | 1-4 x 10^4 |
2. | Opti-MEM Medium | |||
Lipofectamine LTX Reagent | ||||
3. | Opti-MEM Medium | 700uL | 250uL | 125uL |
DNA (0.5-5 ug/uL) | 14ug | 5ug | 2.5ug | |
PLUS Reagent | 14uL | 5uL | 2.5uL | |
4. | Diluted DNA (with PLUS) | 150uL | 50uL | 25uL |
Diluted Lipofectamine LTX | 150uL | 50uL | 25uL | |
6. | DNA-lipid complex (per well) | 250uL | 50uL | 10uL |
FINAL DNA (PER WELL) | 2500ng | 500ng | 100ng |