Figure 6
Figure 6. In vitro fibrinogen binding. Whole blood was drawn into citrate from a retro-orbital sinus of anesthetized animals. Whole blood was stimulated with 10μM ADP, 1 U/mL thrombin, or 1mM MnCl2 and then incubated with Oregon green-fibrinogen for 20 minutes at room temperature. FL1 was read using a FACScan (BD Biosciences). Results are shown for blood from hTgWT animals (black line) and hTgG233V animals (gray line) without agonist or in the presence of ADP, thrombin, or MnCl2. hTgG233V platelets are severely impaired in their ability to respond to either ADP or thrombin.

In vitro fibrinogen binding. Whole blood was drawn into citrate from a retro-orbital sinus of anesthetized animals. Whole blood was stimulated with 10μM ADP, 1 U/mL thrombin, or 1mM MnCl2 and then incubated with Oregon green-fibrinogen for 20 minutes at room temperature. FL1 was read using a FACScan (BD Biosciences). Results are shown for blood from hTgWT animals (black line) and hTgG233V animals (gray line) without agonist or in the presence of ADP, thrombin, or MnCl2. hTgG233V platelets are severely impaired in their ability to respond to either ADP or thrombin.

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