Brief Protocol: |
Mouse splenocytes were isolated by the use of a cell strainer. Approximately 4 · 106 were used for the staining. Cells were first incubated with Biotin anti-mouse CD8 antibody for 10 minutes, were washed once and second staining with Brilliant Violet 510™ SAV was performed for 30 minutes (dilution 1:400). Both stainings were incubated in the dark and at room temperature in a total volume of 50 µl PBS, 0,1% BSA and 0,02% Natriumazid. Cells were washed once and were measured immediately. |
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