Application: |
flow cytometry |
Cells used: |
murine splenocytes, liver lymphocytes, PBMCs |
Brief Protocol: |
1. Prepare single cell suspension of "cells of interest" 2. Use 2-5 million cells/tube (or per well if 96-well plate is used for staining) 3. Centrifuge cells to pellet, wash once with FACS buffer 4. Add surface antibody mix, diluted in FACS buffer (for CD3-ApcCyanine7 use 1:100 dilution) 5. Incubate 15-20 min (RT, dark) 6. Wash cells 1-2 times with FASC buffer, and either proceed to data acquisition or perform standard fixation/permeabilization protocol followed by intracellular antibody staining.
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Results Summary: |
Reliably detects Cd3+ cells in murine splenocytes, liver lymphocytes, PBMCs. |
Additional Notes: |
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