Figure 1
Figure 1. Btk−/− PLCγ2−/− mice have reduced peripheral B-cell populations compared with single mutants. (A) Splenocytes from mice of various genotypes were analyzed via fluorescence-activated cell sorter (FACS) using fluorochrome-conjugated anti-B220 and anti-IgM antibodies. Numbers indicate percentage of cells in lymphocyte gate. Figures shown were representative of at least 4 independent experiments. (B) Enumeration of splenic B cells (mean ± SEM) in various mice. Number of cells is calculated based on total cell count and fraction of B220+IgM+ cells present in the tissues as revealed by FACS staining. Wild-type (WT), n = 6; Btk−/−, n = 6; PLCγ2−/−, n = 5; and Btk−/− PLCγ2−/− (DKO), n = 4.

Btk−/−PLCγ2−/− mice have reduced peripheral B-cell populations compared with single mutants. (A) Splenocytes from mice of various genotypes were analyzed via fluorescence-activated cell sorter (FACS) using fluorochrome-conjugated anti-B220 and anti-IgM antibodies. Numbers indicate percentage of cells in lymphocyte gate. Figures shown were representative of at least 4 independent experiments. (B) Enumeration of splenic B cells (mean ± SEM) in various mice. Number of cells is calculated based on total cell count and fraction of B220+IgM+ cells present in the tissues as revealed by FACS staining. Wild-type (WT), n = 6; Btk−/−, n = 6; PLCγ2−/−, n = 5; and Btk−/−PLCγ2−/− (DKO), n = 4.

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