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. Author manuscript; available in PMC: 2017 Aug 1.
Published in final edited form as: Proteins. 2016 Jun 15;84(8):1162–1172. doi: 10.1002/prot.25062

Figure 2. Binding and toxin-neutralizing activities associated with F5 and F8.

Figure 2

(A) Relative affinities of F5 and F8 for ricin, as determined by direct ELISA in which ricin was captured in its native form on the microtiter plate wells via a surrogate receptor asialofetuin (ASF). EC50 values are defined as the antibody concentration that achieved half-maximal binding. (B) F5 and F8 were mixed at the indicated concentrations with ricin (10 ng/ml) in solution and then applied to Vero cells for cytotoxicity assessment, as described in Materials and Methods. IC50 values were based in the antibody concentration that conferred 50% viability. A single representative experiment done in triplicate is shown. The EC50 and IC50 determinations were done at least three independent times.