Figure 5. Treatment with 20µM Cu10MT-2A or CaMeMT-2A had no protective effect against 40µM Aβ1–40 (in the presence of 40µM CuCl2 and 300µM ascorbate) (A).
Treatment of cortical neurons with 10µM or 100µM H2O2 for two hours resulted in substantial neuronal death, which was not prevented by co-treatment with 20µM Zn7MT-2A (B). Error bars represent standard error of the mean calculated from at least three experimental replicates. In panel A, * - p<0.05 compared to untreated cells (One-Way ANOVA). In panel B, Two-Way ANOVA analysis was performed, and * - p<0.05 compared to untreated cells, # - p<0.05 between treatments.
