Hello,
i am a PhD student and i have to view mitochondrial dynamics in cells, in vitro. can any body tell me that shall i use only mitotracker red or any other dye either in combination with mito red or alone. Or can i use antibodies against cytochrome c and the secondary antibody tagged with red fluorophore?
i am confused, which option is the best and also if i wish to observe mitochondrial morphology in resected tisse, will the protocol be same or?