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. 2010 Aug 11;5(8):e12030. doi: 10.1371/journal.pone.0012030

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).

Figure 5

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.