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. Author manuscript; available in PMC: 2010 Apr 5.
Published in final edited form as: J Cell Sci. 2008 Sep 30;121(Pt 20):3413–3421. doi: 10.1242/jcs.032847

Fig. 4.

Fig. 4

N-terminal CENPF expression localizes to foci containing both TGN and recycling endosome markers. NTmCENPF was transfected into C2C12 cells and markers for SNAREs, TGN and recycling endosomes were immunolabelled. (A) Syntaxin 4 did not colocalize with NTmCENPF-myc, but there was a redistribution of the protein in cells that were transfected. (B-D) SNAP-25, golgin and VAMP2 did colocalize with NTmCENPF. NTmCENPF immunofluorescence is shown in green; endogenous markers are in red. DAPI was used to visualize the nuclei (blue). Bar, 10 μm.