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. Author manuscript; available in PMC: 2021 Mar 31.
Published in final edited form as: Methods Mol Biol. 2021;2270:307–321. doi: 10.1007/978-1-0716-1237-8_17

Fig. 1.

Fig. 1

Cell sorting. Splenocytes are incubated with CD19 microbeads and then naïve CD19+ B cells are enriched through immunomagnetic separation. The frequency of CD19+CD9+ B cells is shown in the plot. Dot plots also show the expression of CD9 and IL-10 in CD19+ B cells which are treated either with LPI for 5 h or with an anti-CD40 antibody for 48 h plus LPI for the last 5 h, after staining with an IL-10 secretion assay kit as described in Subheading 3.1.4. The purity of CD9+IL-10+ and CD9+IL-10 B cells sorted from the cells cultured for 48 h is shown. After sorting, the fluorescence of the sorted cells demonstrates obvious attenuation