Hi, Everyone,
I am doing a screening with fluorescence-activated cell sorting technique. Even after optimization (plus sucrose in the collection tube suggested by Adam Kuspa, rescue and grow cells on KA plate), only ~10% of cells survive through this physical sorting. This makes large-scale screening more difficult.
The cells were sporulated for 24 hours, and then applied to FACS machine.
Any suggestions for further cell viability are welcome.
Thanks, Xin-Hua Liao