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. 2020 Mar 5;10(5):e3544. doi: 10.21769/BioProtoc.3544

Figure 3. Representative fluorescence microscopy images of Myomerger-deficient C2C12 cells used to evaluate the efficiency of lipid mixing by analysis of redistribution of lipid probe (Dil) and content probe (CellTrackerTM Green).

Figure 3.

Images of the cells after co-incubation of Dil-labeled cells with CellTrackerTM green-labeled cells in the differentiation medium. Nuclei are stained by Hoechst. Arrows indicate examples of several distinct phenotypes counted or not counted as mononucleated cells co-labeled with Dil and CellTrackerTM Green. A and B mark colabeled cells with stronger (A) and weaker (B) levels of Dil fluorescence. Cells like the ones marked as A and B were counted as co-labeled mononucleated cells. Cells labeled with only CellTrackerTM Green (C), or only Dil (D), or green cells with just one red point (E) or cells with more than one nucleus (F) were not counted as co-labeled mononucleated cells. Scale bar = 50 μm.