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Lymphoid development in CD48-deficient mice. Thymocytes and splenocytes were purified from CD48+/+ mice (upper row) and from CD48−/− mice (lower row) and were analyzed by dual color immunofluorescence and flow cytometry. All samples were analyzed on a FACScan after compensation. Five-thousand cells were analyzed per sample. Antigens displayed on the y axes were stained with PE-conjugated mAbs whereas antigens on the x axes were stained with fluorescein isothiocyanate-conjugated mAbs.
