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. 2010 Jun 16;73(8):1612–1631. doi: 10.1016/j.jprot.2010.03.018

Fig. 3.

Fig. 3

Western immunoblot of ATP-citrate lyase in liver homogenate from Nrf2(−/−) and Nrf2(+/+) mice. (A) Immunoblot for ATP-citrate lyase in liver homogenate from four Nrf2(−/−) mice (KO1–KO4) and four Nrf2(+/+) mice (WT1–WT4). The molecular mass of ATP-citrate lyase is approximately 120 kDa. (B) Ponceau protein stain of the transfer membrane shown in A) indicating approximately equal loading across the gel. Lane KO1 shows slightly decreased loading which is consistent with the lower level of ATP-citrate lyase in the blot above. (C) Densitometric analysis of immunoblot showing a statistically significant (p < 0.05; Student's t-test) elevation of expression in the Nrf2(−/−) mice compared with the wild type controls.