Skip to main content
. 2008 Dec 10;83(4):1682–1688. doi: 10.1128/JVI.02208-08

FIG. 2.

FIG. 2.

Analysis of PGC1α and CYP4A1 transcripts in the livers of HBV transgenic mice. Mice were fed (control) or fasted for 48 h (fasting). (A) Quantitative analysis of the PGC1α transcript by RT-qPCR in the HBV transgenic mice. The GAPDH transcript was used as an internal control for the quantitation of the PGC1α RNA. The mean relative PGC1α transcript levels plus standard deviations are shown for the following groups of HBV transgenic mice: five control male FoxA3+/−, six fasted male FoxA3+/−, eight control male FoxA3−/−, and seven fasted male FoxA3−/− mice. The levels of the PGC1α transcript in the fasted HBV transgenic mice are statistically significantly different from their levels in the control HBV transgenic mice by a Student's t test (P < 0.05). (B) RNA (Northern) filter hybridization analysis of CYP4A1 transcripts in the livers of HBV transgenic mice. Groups of four representative male mice of each genotype are shown. The GAPDH transcript was used as an internal control for the quantitation of the CYP4A1 RNA. The probes used were CYP4A1 plus GAPDH cDNA.