Fig. 2.
Fig. 2. Mixing patient plasma with normal plasma generates TAT′ complex and impairs residual prothrombin activity. / (A) Mixtures of patient plasma (0%, ▪; 5%, ●; 10%, ▴; 50% final, ♦) and normal plasma were incubated at 37°C for 0 to 24 hours. The amount of TAT′ complex generated in each sample was measured by ELISA for normal TAT. (inset) TAT complex and TAT′ complex isolated from patient plasma were subjected to SDS-PAGE (10% separating gels under reducing conditions). (B) Patient plasma (0%, ▪; 5% final, ●) was mixed with normal plasma and incubated at 37°C for 0 to 24 hours. Residual prothrombin activity in each sample was measured.

Mixing patient plasma with normal plasma generates TAT′ complex and impairs residual prothrombin activity.

(A) Mixtures of patient plasma (0%, ▪; 5%, ●; 10%, ▴; 50% final, ♦) and normal plasma were incubated at 37°C for 0 to 24 hours. The amount of TAT′ complex generated in each sample was measured by ELISA for normal TAT. (inset) TAT complex and TAT′ complex isolated from patient plasma were subjected to SDS-PAGE (10% separating gels under reducing conditions). (B) Patient plasma (0%, ▪; 5% final, ●) was mixed with normal plasma and incubated at 37°C for 0 to 24 hours. Residual prothrombin activity in each sample was measured.

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