Figure 1.

Co-localization of ML1 with markers for various compartments. A) Confocal images of stable GFP-ML1 (green) cells stained for the indicated markers (red). The inset in the LBPA panels is a magnification of individual compartments. Bar is 10 μm. B) Quantitation of the fraction of GFP-ML1 stainings that overlaps with each of the markers from panel A. Bars represent standard deviations. C) Confocal images of cells co-transfected with mCherry-ML1 (mCH-ML1, red) and with GFP or YFP fusions to the indicated markers (green). Bar is 10 μm. D) Quantitation of the fraction of mCherry-ML1 stainings that overlaps with each of the markers from panel C. Bars represent standard deviations.

Thompson et al. BMC Cell Biology 2007 8:54   doi:10.1186/1471-2121-8-54
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