I am working on yeast surface display library. After I work with yeasts for a while, I obviously see them at very bad conditions.
If I let the media stand for 1 min, I see cells aggregate very fast, form weird turbid media, and precipitate to the bottom super fast.
I assume it might be because the freezing with DMSO was harmful? But I honestly followed every step from a published protocol, so what could be the reason and what should I do?