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. 2009 Feb 27;37(6):1295–1304. doi: 10.1124/dmd.108.025213

Fig. 5.

Fig. 5.

PXR.2 can compete with PXR.1 for rifampin activation of reporter plasmids. HepG2 cells were transfected with expression vectors encoding PXR.1 or PXR.2 (A and B) pCMX-Gal4-PXR or pMSCV-hPXR-IRES-GFP (C and D) with appropriate reporter genes as described under Materials and Methods and treated for 48 h with 10 μM rifampin and relative reporter activity graphed relative to cells without cotransfected PXR. B and D, a constant amount of PXR.1 (10 ng) was cotransfected with increasing amounts of PXR.2 and the reporter plasmids. Values represent the mean ± S.D. measured in triplicate in at least two independent transfections. The ratio of PXR.2 to PXR.1 expression plasmid was graphed relative to activation of reporter genes.