Table 1. Transcriptional activation by transiently transfected tetracycline-dependent transactivators.
Cell line | Plasmid transfected with | std. RLU | x-fold induction | |
|
pUHC13-3 |
Doxy(–) |
Doxy(+) |
|
HeLa | pUHD172-1neo | 2.72 | 335.31 | 123.2 |
prTE 4d38-neo | 1.22 | 38.25 | 31.4 | |
Cos-7 | pUHD172-1neo | 29.4 | 1226.7 | 41.7 |
prTE 4d38-neo | 20.0 | 565.9 | 28.3 | |
NIH 3T3 | pUHD172-1neo | 8.75 | 687.8 | 78.6 |
prTE 4d38-neo | 2.52 | 132.1 | 52.4 |
pUHC13-3 and pRL-CMV (Renilla luciferase expression vector) were co-transfected with pUHD172-1 or prTE4d38 into 1–3 × 105 cells. Cultures were incubated in the presence or absence of doxycycline for 24 h before luciferase activity was measured and standardized to Renilla luciferase activity. Induction ratios were estimated by standardized basal levels of luciferase activities [std. RLU, Doxy(–)] and standardized induced levels of luciferase activities [std. RLU, Doxy(+)]. Doxy(+) or (–), presence or absence of doxycycline, respectively. Results were the average from three experiments.