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Found 1 matching solution for this experiment
pBud-hIL-7
Abbas Ghaderi, Shiraz Institute for Cancer Research, School of M
Upstream tips |
Protocol tips |
Downstream tips |
The CHO-K1 cells were passaged 24 h before the transfections and harvested at 75-85% confluency on the day of transfection. |
For stable transfections, 5×105 cells and 20 µg of each plasmid (either circular plasmid or plasmid linearized with XhoI) were used at 350 V and 950 µF in a Gene Pulser Xcell electroporation system (Bio-Rad, CA, USA) using a single exponentially-decaying pulse. The electroporated cells were recovered in a shaking flask containing growth medium. |
At 48 h after electroporation, cell viability was measured by trypan blue exclusion on a hemocytometer, and supernatants were collected for IL-7 expression analyses using the enzyme-linked immunosorbent assay (ELISA). Transfected cells were cultured with complete medium supplemented with 600 µg/ml of Zeocin. Pools of stable clones were assayed after 14 days of selection. The amount of protein in the supernatant was assessed by the Bradford protein assay (20). |
Upstream tips |
The CHO-K1 cells were passaged 24 h before the transfections and harvested at 75-85% confluency on the day of transfection. |
Protocol tips |
For stable transfections, 5×105 cells and 20 µg of each plasmid (either circular plasmid or plasmid linearized with XhoI) were used at 350 V and 950 µF in a Gene Pulser Xcell electroporation system (Bio-Rad, CA, USA) using a single exponentially-decaying pulse. The electroporated cells were recovered in a shaking flask containing growth medium. |
Downstream tips |
At 48 h after electroporation, cell viability was measured by trypan blue exclusion on a hemocytometer, and supernatants were collected for IL-7 expression analyses using the enzyme-linked immunosorbent assay (ELISA). Transfected cells were cultured with complete medium supplemented with 600 µg/ml of Zeocin. Pools of stable clones were assayed after 14 days of selection. The amount of protein in the supernatant was assessed by the Bradford protein assay (20). |
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