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. 2006 May 23;103(23):8804–8809. doi: 10.1073/pnas.0603043103

Fig. 4.

Fig. 4.

Flow cytometric analysis of binding activity of mAbP and mAbM BR55-2 to the FcγRI receptor. (A) U937 cells treated with IFN-γ to stimulate Fc receptor expression were incubated with mAbP or mAbM BR55-2 or CD64-specific mAb m22-FITC. Binding activity of mAbP (Left), mAbM (Center), and m22-FITC (Right) to the activated cells expressing CD64 were analyzed by flow cytometry. Black and gray lines indicate binding of mAbs before or after blocking treatment of human serum, respectively (Left and Center) or indicate cells treated with m22-FITC or an mAb isotype control (Right). (B) 3T3 cells were transfected with CD64 cDNA and treated with mAbP BR55 (Left), mAbM BR55 (Center), or mAb m22-FITC (Right). Black and gray lines indicate transfected or mock-transfected cells bound by each mAb, respectively.