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Found 1 matching solution for this experiment
pCEP-4-MBP
Manuel Koch, Institute for Dental Research and Oral Musculoskele
Upstream tips |
Protocol tips |
Downstream tips |
HEK293 cells were seeded at 90% confluency in a 24-well plate and allowed to adhere overnight. |
Next day, cells were transfected with different constructs in triplicates using FuGENE® HD (Promega, Mannheim, Germany, Cat. no.: E2311). FuGENE® HD was added to DMEM/F-12, GlutaMAX™ (Life Technologies, Darmstadt, Germany, Cat. no: 10565–018) at RT for 10 min and then incubated with different plasmid DNA for additional 20 min. The transfection reagent to plasmid DNA ratio was 1:3 (0.5 μg plasmid per well). The different transfection DNA mixtures were directly added to the respective wells and incubated for 24 h. |
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Upstream tips |
HEK293 cells were seeded at 90% confluency in a 24-well plate and allowed to adhere overnight. |
Protocol tips |
Next day, cells were transfected with different constructs in triplicates using FuGENE® HD (Promega, Mannheim, Germany, Cat. no.: E2311). FuGENE® HD was added to DMEM/F-12, GlutaMAX™ (Life Technologies, Darmstadt, Germany, Cat. no: 10565–018) at RT for 10 min and then incubated with different plasmid DNA for additional 20 min. The transfection reagent to plasmid DNA ratio was 1:3 (0.5 μg plasmid per well). The different transfection DNA mixtures were directly added to the respective wells and incubated for 24 h. |
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