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. 2000 Jun 20;97(14):7963–7968. doi: 10.1073/pnas.130192197

Table 2.

Response of rtTA and of the new rtTA variants toward Dox

Dox, ng/ml Response in arbitrary light units of rtTA alleles
rtTA S2 19/56R M1 M2
0 0.67  ± 0.28 1.24  ± 0.41 0.62  ± 0.48 2.54  ± 2.05 1.02  ± 1.16 3.02  ± 1.26
5 0.52  ± 0.06 57.27  ± 6.66 1.26  ± 0.17 3.24  ± 2.72 1.24  ± 1.54 17.07  ± 5.58
50 0.64  ± 0.55 229.72  ± 35.34 26.52  ± 12.4 0.91  ± 0.32 30.94  ± 25.75 1,517.37  ± 169.94
500 0.94  ± 0.63 696.27  ± 70.3 1,726.75  ± 110.64 112.68  ± 6.98 2,428.19  ± 254.42 10,746.33  ± 1,272.97

Dox-dependent gene activation of various rtTAs was measured in HeLa X1/6 cells that were transiently transfected with plasmids containing the genes for the transactivators rtTA and rtTA-S2, -19/56R, -M1, and -M2, all of which were controlled by PCMV. For standardization of transfection efficiencies, each transfection mixture contained also a vector that constitutively produces β-galactosidase. Cells were grown in absence of or in presence of 5, 50, and 500 ng/ml Dox. Twenty-four hours post transfection, luciferase activity was measured from cell extracts and normalized to β-galactosidase activity. Values given are arbitrary light units.