Fig. 2.
Fig. 2. Concentration dependence of FGF-1, -2, -4, -6 binding to α2M and α2M*. / A total of 15 ng 125I–FGF-1 (A), 125I–FGF-2 (B), 125I–FGF-4 (C), or 125I–FGF-6 (D) was incubated with varying concentrations of α2M (●) or α2M* (▪) for 2 hours at 37°C followed by nondenaturing pore-limit electrophoresis. Radioactivity was quantified on a Phosphorimager and represented by arbitrary units (AU). Binding and lines that represent the best least square fit (R2 > 0.95) are plotted in the figure. The data are representative of 3 (FGF-1 and FGF-6) or 4 (FGF-2 and FGF-4) experiments. Table 1 contains a summary of theKd values derived from these binding experiments.

Concentration dependence of FGF-1, -2, -4, -6 binding to α2M and α2M*.

A total of 15 ng 125I–FGF-1 (A), 125I–FGF-2 (B), 125I–FGF-4 (C), or 125I–FGF-6 (D) was incubated with varying concentrations of α2M (●) or α2M* (▪) for 2 hours at 37°C followed by nondenaturing pore-limit electrophoresis. Radioactivity was quantified on a Phosphorimager and represented by arbitrary units (AU). Binding and lines that represent the best least square fit (R2 > 0.95) are plotted in the figure. The data are representative of 3 (FGF-1 and FGF-6) or 4 (FGF-2 and FGF-4) experiments. Table 1 contains a summary of theKd values derived from these binding experiments.

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