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. Author manuscript; available in PMC: 2013 Feb 1.
Published in final edited form as: J Neurosci. 2012 Aug 1;32(31):10587–10593. doi: 10.1523/JNEUROSCI.0015-12.2012

Fig 1.

Fig 1

Localization of RHO and kinesin-2/IFT proteins in cilia of hTERT-RPE1 cells. (A, B) Fluorescence micrographs of cells transiently transfected with RHO-EGFP (A) and IFT88-YFP (B). (C, D) Immunofluorescence micrographs, showing endogenous heterotrimeric kinesin-2, as indicated by KAP3 labeling (C), and homodimeric kinesin-2, as indicated by KIF17 labeling (D). Adjacent panels show immunfluorescence of acetylated α-tubulin, a cilium marker (red), and colocalizations shown as shifted overlays. Nuclei were stained with DAPI (blue). Scale bars = 10μm.