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Splenocytes from C57BL/6 mice were stained with CD19 antibodies. Cells were then fixed and permeabilized using the FoxP3 Staining Buffer Set and stained with Anti-Aiolos antibodies or with the corresponding REA Control antibodies (left image). Flow cytometry was performed using the MACSQuant®
Analyzer. Cell debris were excluded from the analysis based on scatter signals.
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