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

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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 150uL x 4 50uL 25uL x 4
Lipofectamine LTX Reagent  6, 9, 12, 15 uL1.5uL1, 1.5, 2, 2.5 uL 
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

 

In blue: To be tested