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. Author manuscript; available in PMC: 2012 Jul 15.
Published in final edited form as: Toxicol Appl Pharmacol. 2011 Feb 15;254(2):65–71. doi: 10.1016/j.taap.2010.03.023

Fig. 3.

Fig. 3

Cytotoxicity of acute MnCl2 treatment in differentiated N27 cells. Differentiated N27 cells were treated with 3 μM or 10 μM MnCl2 for 3 h. The effect of acute manganese treatment on cell death was quantified by Sytox Green fluorescence assay. The intensity of fluorescence was measured by fluorescence plate reader and shown as % of control. N27 cells exposed to 100 μM H2O2 for 3 h were used as a positive control. The data represent a mean + SEM of four individual measurements. Asterisks (***p<0.001) indicate significant differences between H2O2-treated cells and control cells.