Application: |
Flow cytometry phenotyping of mouse spleen and LNs |
Cells used: |
Mouse lymphocytes |
Brief Protocol: |
Cells were stained for 30minutes with CD44 APC Fire 750 at a dilution of 1:100 in 50uL of FACS buffer. The cells were then washed 2x and fixed with 2% PFA for 30mins or with ebioscience fixation buffer (for Foxp3 staining) overnight. The cells were then washed and run on a flow cytometer or were permeabilized the next day for Foxp3 staining after which they were washed and run on a flow cytometer. |
Results Summary: |
Both dilutions of 1:100 and 1:50 worked very well. There was no disintergration of APC Fire 750 into APC. This really helped use the same flurochrome for both surface and transcription factor panels. I wasn't able to do this before when I used CD44 APC efluor 780. |
Additional Notes: |
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