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STEPS:
  1. One day before transfecting, seed cells (in a well plate) so that they are 70-90% confluent at time of transfection.
  2. Dilute Lipofectamine LTX Reagent in Opti-MEM Medium (Ratio = 
  3. Dilute DNA in Opti-MEM Medium, then add PLUS Reagent (Ratio = 50uL Opti-MEM: 1ug DNA: 1uL PLUS).
  4. Add diluted DNA to diluted Lipofectamine LTX Reagent in a 1:1 ratio.
  5. Incubate at room temperature for 5 minutes.
  6. Add DNA-lipid complex to cells.
  7. Incubate cells for 1-3 days at 37C.
  8. Visualize/analyze transfected cells (flow cytometry).


n-WELL PLATE PROPORTIONS:

STEPCOMPONENT6-well24-well96-well
1.Adherent Cells0.25-1 x 10^60.5-2 x 10^51-4 x 10^4
2.Opti-MEM Medium   
Lipofectamine LTX Reagent   
3.

Opti-MEM Medium700uL250uL125uL
DNA (0.5-5 ug/uL)14ug5ug2.5ug
PLUS Reagent14uL5uL2.5uL
4.Diluted DNA (with PLUS)150uL50uL25uL
Diluted Lipofectamine LTX150uL50uL25uL
6.DNA-lipid complex (per well)250uL50uL10uL
FINAL DNA (PER WELL)2500ng500ng100ng
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