I have started doing flow experiments to count neutrophils in murine spleens.
Who can help me designing a good gating strategy for it? I'm using CD11b and Gr-1 as markers (and of course a live/death dye) now. I will introduce a Ly6G marker since it is specific for neutrophils, but is it possible to get a clear neutrophil population with the previous 2 markers?
Thank you in advance!
Giulia