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. Author manuscript; available in PMC: 2010 Jan 31.
Published in final edited form as: Toxicology. 2008 Nov 6;255(3):171–176. doi: 10.1016/j.tox.2008.10.020

Figure 2.

Figure 2

SERCA and CYP2E1 expression in C34 and E47 cells. Microsomes derived from C34 or E47 cells were loaded (30 μg prot) in a SDS-polyacrylamide gel, and western-blotted using anti-SERCA 1,2,3 (A) or anti-CYP2E1 antibodies (B). Protein Gβ was used as microsomal loading control.