Fig. 2.
Fig. 2. Phenotype of CD45R+CD43+ pro–B cells following culture on S17 stromal cells or in FTOCs. / (A) 5 × 104 CD45R+sIgM− cells were seeded into FTOCs or onto S17 stroma. Cells were phenotyped 7 days later as described in Figure 1. (B) 2.5 × 104fluorescence-activated cell-sorter (FACS)–purified CD45R+CD43+ pro–B cells were seeded into FTOCs. Phenotypic analysis was performed on cells harvested from lobes 7 days after initiation of cultures. Data in the figures are representative of 3 experiments.

Phenotype of CD45R+CD43+ pro–B cells following culture on S17 stromal cells or in FTOCs.

(A) 5 × 104 CD45R+sIgM cells were seeded into FTOCs or onto S17 stroma. Cells were phenotyped 7 days later as described in Figure 1. (B) 2.5 × 104fluorescence-activated cell-sorter (FACS)–purified CD45R+CD43+ pro–B cells were seeded into FTOCs. Phenotypic analysis was performed on cells harvested from lobes 7 days after initiation of cultures. Data in the figures are representative of 3 experiments.

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