The experiment was set up in the same way as that described in “p38 MAPK overexpression by plasmid transfection” with the following modifications. Cells were seeded at a concentration of 2 × 104 cells/100 μL of relevant medium (see above) into the wells of the 96-well plate. The amount of plasmid DNA used was 100 ng per well. After 48 h of incubation with or without SA, the number of living cells was determined using a hemocytometer counting system after staining with trypan blue.
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