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. Author manuscript; available in PMC: 2016 Jun 13.
Published in final edited form as: J Cell Biochem. 2008 Aug 15;104(6):2217–2227. doi: 10.1002/jcb.21780

Fig. 6.

Fig. 6

Recording of cytoplasmic Ca2+ in cultured chick cardiomyocytes using Rhod-2 AM calcium indicator. Changes in cytoplasmic Ca2+ were tracked over time by observing the increase in cytoplasmic fluorescence from time 0 to the peak of the Ca2+ transient (0.5 s), and decrease back to baseline. Arrow points to cytoplasmic region of interest (ROI). ROI's were chosen to avoid Rhod-2 accumulation within organelles, which appear as bright spots within the cell monolayer (Materials and Methods). Representative images are from ATP control following hypertonic loading at 25°C.