Fig. 7.
Fig. 7. Plasminogen activation on LM-TK− cells. LM-TK− cells (filled bars) and their extracellular matrix (hatched bars) were incubated in the absence or presence of uPA (10 nmol/L), as well as in the absence or presence of suPAR (1 μg/mL) and MoAb-13H1 (25 μg/mL) against VN for 2 to 3 hours at 4°C as indicated. The unbound uPA was then washed away and the rate of plasmin formation was measured (Vmax, mOD/min at 405 nm). Results are mean ± SEM of triplicate wells and similar results were obtained in three separate experiments.

Plasminogen activation on LM-TK cells. LM-TK cells (filled bars) and their extracellular matrix (hatched bars) were incubated in the absence or presence of uPA (10 nmol/L), as well as in the absence or presence of suPAR (1 μg/mL) and MoAb-13H1 (25 μg/mL) against VN for 2 to 3 hours at 4°C as indicated. The unbound uPA was then washed away and the rate of plasmin formation was measured (Vmax, mOD/min at 405 nm). Results are mean ± SEM of triplicate wells and similar results were obtained in three separate experiments.

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