Abstract
A method is described in which thrombin activity in clotting plasma can be monitored through the continuous measurement of the fluorescent split-product of the substrate Z-Gly-Gly-Arg-AMC. The signal is not impaired by turbidity; therefore proper measurement is not disturbed by the occurrence of a clot or the presence of platelets and direct measurement in platelet rich plasma is possible.
Original language | English |
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Pages (from-to) | 589-591 |
Journal | Thrombosis and Haemostasis |
Volume | 83 |
DOIs | |
Publication status | Published - 1 Jan 2000 |