Hi all,
I am attempting to use several fluorescent probes to evaluate various aspects of mitochondrial metabolism in neutrophils.
When I use my JC-1 probe it immediately clumps into sediment when I introduce it to my medium, and no amount of vortexing can dissolve these clumps.
For context, the probe is dissolved in DMSO at a 5mg/ml conc, and I dilute that into a 5ug/ml conc in complete RPMI media.
Any advice?