▲ 2 r/flowcytometry
Compensation with Proliferation Dyes
Hi,
I am running a T-cell proliferation exp and am unsure how to best compensate with CFSE.
My data came out strange and I am wondering if it is due to using beads for all other comp, and cells (50% stained 50% unstained) for comp of CFSE. Would this be the best way to go about it? Or can I run beads with a FITC stain and comp that way?
I am trying to trouble shoot multiple things at once so it is a challenging. Thanks in advance!
u/GrindIsAlwaysReal — 13 days ago