Figure 6.
Figure 6. Redistribution of band 3 on normal and ankyrin-deficient (nb/nb) red cells. (A) Fluorescence micrograph of normal erythrocyte with EMA-labeled band 3 aspirated by a micropipette. (B) Corresponding intensity profile of band 3 exhibited a steep gradient in concentration along the deformation projection, indicating that the density of EMA-labeled band 3 increased markedly at the pipette entrance and subsequently decreased toward the aspiration cap. ρe and ρc are defined as the densities at the pipette entrance and at the cap of the projection, respectively. (C) Fluorescence micrograph of ankyrin-deficient erythrocyte with EMA-labeled band 3 aspirated by a micropipette. (D) Without ankyrin, band 3 collected at the cap as seen by the reverse gradient and higher fluorescence intensity at the cap. For scale reference for panels A and C, the diameter of the micropipette is 0.8 μm.

Redistribution of band 3 on normal and ankyrin-deficient (nb/nb) red cells. (A) Fluorescence micrograph of normal erythrocyte with EMA-labeled band 3 aspirated by a micropipette. (B) Corresponding intensity profile of band 3 exhibited a steep gradient in concentration along the deformation projection, indicating that the density of EMA-labeled band 3 increased markedly at the pipette entrance and subsequently decreased toward the aspiration cap. ρe and ρc are defined as the densities at the pipette entrance and at the cap of the projection, respectively. (C) Fluorescence micrograph of ankyrin-deficient erythrocyte with EMA-labeled band 3 aspirated by a micropipette. (D) Without ankyrin, band 3 collected at the cap as seen by the reverse gradient and higher fluorescence intensity at the cap. For scale reference for panels A and C, the diameter of the micropipette is 0.8 μm.

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