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Found 2 matching solutions for this experiment
pcDNA-oGP1
Peter D. Sun, Structural Immunology Section, Laboratory of Immun
Upstream tips |
Protocol tips |
Downstream tips |
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For transient expression, a T-25 flask was seeded with 1 ×106 293T cells one day before the transfection. Six μg of pcDNA-nGP1 or pcDNA-oGP1 was diluted into 0.3 ml OPTI-MEM I reduced serum medium and 24 μl of FuGENE® HD Transfection Reagent (Promega, Madison, WI) was then added into the solution. The transfection reagent and DNA mix was incubated for 20 min at room temperature, then added into the T-25 flask. |
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Protocol tips |
For transient expression, a T-25 flask was seeded with 1 ×106 293T cells one day before the transfection. Six μg of pcDNA-nGP1 or pcDNA-oGP1 was diluted into 0.3 ml OPTI-MEM I reduced serum medium and 24 μl of FuGENE® HD Transfection Reagent (Promega, Madison, WI) was then added into the solution. The transfection reagent and DNA mix was incubated for 20 min at room temperature, then added into the T-25 flask. |
pcDNA-nGP1
Peter D. Sun, Structural Immunology Section, Laboratory of Immun
Upstream tips |
Protocol tips |
Downstream tips |
|
For transient expression, a T-25 flask was seeded with 1 ×106 293T cells one day before the transfection. Six μg of pcDNA-nGP1 or pcDNA-oGP1 was diluted into 0.3 ml OPTI-MEM I reduced serum medium and 24 μl of FuGENE® HD Transfection Reagent (Promega, Madison, WI) was then added into the solution. The transfection reagent and DNA mix was incubated for 20 min at room temperature, then added into the T-25 flask. |
|
Protocol tips |
For transient expression, a T-25 flask was seeded with 1 ×106 293T cells one day before the transfection. Six μg of pcDNA-nGP1 or pcDNA-oGP1 was diluted into 0.3 ml OPTI-MEM I reduced serum medium and 24 μl of FuGENE® HD Transfection Reagent (Promega, Madison, WI) was then added into the solution. The transfection reagent and DNA mix was incubated for 20 min at room temperature, then added into the T-25 flask. |
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