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. 2017 Jul 15;136:62–75. doi: 10.1016/j.bcp.2017.04.006

Fig. 4.

Fig. 4

Inhibition of the binding of VEGF165a-TMR to NLuc-VEGFR2 by unlabeled VEGF isoforms. Fixed concentrations of VEGF165a-TMR (0.1–3 nM) were added simultaneously with increasing concentrations of (a) VEGF165b, (b) VEGF121a, (c) VEGF145a and (d) VEGF189a, and incubated for 1 h at 37 °C. Data represent mean ± S.E.M of 5 independent experiments, each performed in triplicate. Bars represent the binding of VEGF165a-TMR obtained at each fluorescent ligand concentration in the absence of competing ligand. The open bar shows the BRET ratio obtained in the absence of VEGF165a-TMR.