Fig. 5.
Fig. 5. Effect of echicetin (A) and echistatin (B) on CHO cells transfected with either vβ3 or GPIb complex. A 96-well microplate was coated with vWF. Confluent CHO cells transfected with either vβ3 (•) or GPIbβIX (▪) were detached with Versene (GIBCO) for 30 minutes at 37°C. After washing with PBS, the cells were resuspended in PBS containing 1 mmol/L CaCl2 and MgCl2. The concentration of the cell suspension was adjusted to 2 × 105 cells/mL. Varying concentrations of echicetin and echistatin were added to 100 μL aliquots of the cell suspension 15 minutes before 2 hours of incubation on the plate. Unbound cells were gently washed away with PBS. The adhesion procedure was followed according to the legend of Fig 2.

Effect of echicetin (A) and echistatin (B) on CHO cells transfected with either vβ3 or GPIb complex. A 96-well microplate was coated with vWF. Confluent CHO cells transfected with either vβ3 (•) or GPIbβIX (▪) were detached with Versene (GIBCO) for 30 minutes at 37°C. After washing with PBS, the cells were resuspended in PBS containing 1 mmol/L CaCl2 and MgCl2. The concentration of the cell suspension was adjusted to 2 × 105 cells/mL. Varying concentrations of echicetin and echistatin were added to 100 μL aliquots of the cell suspension 15 minutes before 2 hours of incubation on the plate. Unbound cells were gently washed away with PBS. The adhesion procedure was followed according to the legend of Fig 2.

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