Fig. 5.
Fig. 5. Factor Va inactivation by GD-APC is inhibited by prothrombin in the absence of phospholipid. Factor Va (100 nmol/L) was incubated at 37°C in 0.15 mol/L NaCl, 5 mmol/L CaCl2, 20 mmol/L HEPES, pH 7.5, 0.1% gelatin with 10 nmol/L GD-APC in the absence or presence of different prothrombin concentrations. The reaction was stopped at the times indicated by addition of 10 mmol/L benzamidine HCl. The residual factor Va was measured with a 1-stage clotting assay using factor V–deficient plasma. The prothrombin concentrations present were: •, no prothrombin; □, 1.4 μmol/L prothrombin; ○, 10 μmol/L prothrombin. Bars represent the standard deviation of 2 experiments, duplicate samples.

Factor Va inactivation by GD-APC is inhibited by prothrombin in the absence of phospholipid. Factor Va (100 nmol/L) was incubated at 37°C in 0.15 mol/L NaCl, 5 mmol/L CaCl2, 20 mmol/L HEPES, pH 7.5, 0.1% gelatin with 10 nmol/L GD-APC in the absence or presence of different prothrombin concentrations. The reaction was stopped at the times indicated by addition of 10 mmol/L benzamidine HCl. The residual factor Va was measured with a 1-stage clotting assay using factor V–deficient plasma. The prothrombin concentrations present were: •, no prothrombin; □, 1.4 μmol/L prothrombin; ○, 10 μmol/L prothrombin. Bars represent the standard deviation of 2 experiments, duplicate samples.

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