Fig. 2.
Fig. 2. CD59 expression on erythrocytes of CD59+/+, CD59+/−, and CD59−/− mice. / Erythrocytes were isolated by centrifugation, labeled with a biotinylated anti-CD59 mAb followed by phycoerythrin-conjugated streptavidin, and gated on the forward scatter versus side scatter dot plot generated by the FACSCalibur. (A) Overlay of the histogram profiles of CD59+/+ (unshaded), CD59+/−(lightly shaded), and CD59−/− (heavily shaded) erythrocytes. (B) Graph showing the CD59 mean cell fluorescence (MCF) obtained for erythrocytes from CD59+/+, CD59+/−, and CD59−/− mice (filled bars; 3 in each group). The negative controls shown underwent the same procedure but without the anti-CD59 mAb being present (open bars). Error bars represent SD for the 3 determinations.

CD59 expression on erythrocytes of CD59+/+, CD59+/−, and CD59−/− mice.

Erythrocytes were isolated by centrifugation, labeled with a biotinylated anti-CD59 mAb followed by phycoerythrin-conjugated streptavidin, and gated on the forward scatter versus side scatter dot plot generated by the FACSCalibur. (A) Overlay of the histogram profiles of CD59+/+ (unshaded), CD59+/−(lightly shaded), and CD59−/− (heavily shaded) erythrocytes. (B) Graph showing the CD59 mean cell fluorescence (MCF) obtained for erythrocytes from CD59+/+, CD59+/−, and CD59−/− mice (filled bars; 3 in each group). The negative controls shown underwent the same procedure but without the anti-CD59 mAb being present (open bars). Error bars represent SD for the 3 determinations.

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