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. Author manuscript; available in PMC: 2013 Apr 17.
Published in final edited form as: J Am Coll Cardiol. 2012 Apr 17;59(16):1426–1437. doi: 10.1016/j.jacc.2011.12.033

Figure 7.

Figure 7

In vitro clot lysis assay assessing the ability of plasminogen to degrade fibrin clots. Native plasminogen containing OxPL and plasminogen with OxPL enzymatically removed (inset) with phospholipase A2 were used. In this system, thrombin-induced clot formation occurs within the first 2 min and is marked by an initial rapid increase in turbidity, as measured by absorbance at 405 nm. Subsequent clot lysis is indicated by a rapid return of the turbidity signal to base-line levels. The parameter tm (transition midpoint) is taken as the standard measure of lysis time and is defined as the time point on the lysis curve that is halfway between the minimum and maximum excursions. The curves represent the mean±SEM of 3 separate experiments with measurement of absorbance at 405 nm every 5 seconds.