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. 2012 Feb 21;109(10):3903–3908. doi: 10.1073/pnas.1120160109

Fig. 2.

Fig. 2.

Lymphocyte development defects in 53BP1−/−XLF−/− mice are due to impaired V(D)J recombination. (A) Representative flow cytometric analyses of bone marrow and spleen from WT, XLF−/−53BP1−/−, 53BP1−/−XLF−/−HL, and 53BP1−/−XLF−/−EμBcl2+ mice. Numbers on the plot are percentage of total live cells (determined by forward and side scatter) represented by indicated population. (B) The number of total DN and single-positive (SP) thymocytes and IgM+ splenic B cells were calculated based on total organ cellularity and the percentage of the given cell type (by flow cytometric analyses). Each value listed represents the average ± SD from at least three mice of each genotype between 4 and 12 wk of age. The P values are calculated between corresponding groups by using two-tailed Student's t test. The original data are provided in Fig. S2.