Here there is a kit pritocol
https://www.sigmaaldrich.com/content/dam/sigma-aldrich/docs/Sigma/Bulletin/2/mak156bul.pdf
Why there is no data about application of such kind of protocol for yeast?
I cultivated cells in flasks, washed with PBS and inoculated with Dye Loading solution. Result was strange: very low fluorescence level, decreasing (not increasing) in time.
What is wrong?
Thank you in advance!