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. 2008 Feb 4;105(6):2088–2093. doi: 10.1073/pnas.0705657105

Fig. 3.

Fig. 3.

vl subcellular localization. Double labeling for WT (A and C) and vlGpr161 (B and D) with either the endosome marker, FITC-transferrin (A and B), or plasma membrane-targeted GFP (C and D) was performed for permeabilized transiently transfected HEK293T cells. wtGpr161 is localized to the endosome compartment, whereas vlGpr161 remains on the plasma membrane, consistent with the C-terminal tail truncation affecting receptor-mediated endocytosis of the Gpr161. Confocal microscopy of ≈0.5-μm optical sections through transfected cells is shown. (Scale bar: 10 μm.)