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. 2015 Jun 17;38(7):657–662. doi: 10.14348/molcells.2015.0083

Fig. 2.

Fig. 2.

Subcellular localization of the Ucp2 mutants. (A) Schematic diagram of Ucp2 illustrating the positions of Ucp2 mutations. Large black dot, proton leak mutations; open circle, chloride transport mutation; small black dot, nucleotide-binding mutation. (B) LR73 cells were transfected with the indicated plasmids, lysed, and protein expression analyzed by immunoblotting. The expression of Ucp2 and mutated Ucp2 proteins were detected by immunoblotting. β-actin was used as a loading control. The numbers under the FLAG blot indicate relative expressions of the proteins to Ucp2. (C) LR73 cells, expressing the indicated proteins, were stained with anti-FLAG and AIF antibody. Scale bar, 20 μm.