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ConA induces IL-2Rα expression in absence of active STAT factors. T lymphocytes from IFN-γR-deficient (−/−) or wild-type (WT) mice were stimulated for 24 h with ConA in the presence of the IL-2-blocking MAbs. (A) Flow cytometric analysis of IL-2Rα expression on T cells. (B) Bandshift assay with 3 μg of nuclear extracts incubated with the FcγRI probe for 15 min.
