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FGFR3-binding phages displaying FGF1 mimotopes as characterized by an indirect ELISA. Serial dilutions of phages were incubated with the bound FGFR3 receptor, followed by incubation with a rabbit anti-phage IgG and an HRP-conjugated goat anti-rabbit IgG. Signal was produced using a TMB substrate and endpoint absorbance at 450 nm was measured after a 30-min incubation. Candidate FGFR3-binding phages were compared to the wildtype fd-tet phage (dark green).
