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. Author manuscript; available in PMC: 2013 Nov 29.
Published in final edited form as: J Neurosci. 2013 May 29;33(22):9508–9519. doi: 10.1523/JNEUROSCI.5689-12.2013

Figure 5.

Figure 5

Co-localization of AP-2 protein and myosin VI in mature (P19) IHCs. A Co-localization of myosin VI (red) and AP-2 (green) labeling was found ubiquitously throughout the IHC except the cuticular plate. Cell nuclei were counterstained with DAPI. Scale bar, 5 μm. B-D To better display co-localization, merged images are shown displaying magnifications of single layers out of the deconvoluted z-stack in (A), where (B) and (E) are derived from the supranuclear area (closed arrow in A, merge), (C) and (F) from the base (open arrow in A, merge), and D and G from a vertical cut. Scale bars, 2 μm. E-G Normalized intensity profiles are drawn from the white lines in (B-D) and show the relative pixel intensity along the line with regards to the distance and fluorescence wave length (red, Cy3; green, Alexa488). Co-localization was analyzed by coinciding of maxima of the red and green channel by Pearson correlation (Pearson correlation coefficient, PCC). Images display maximum intensity projections of all layers of a z-stack.