Skip to main content
. 2015 Nov 4;6:648–655. doi: 10.1016/j.redox.2015.10.010

Fig. 2.

Fig. 2.

AFN-induced developmental defects. (A) Images of Tg(gata1:DsRed) embryos at 2 dpf (dorsal view) in which the blood is labeled by DsRed fluorescence, DMSO control is top and 5 µM AFN is bottom. Arrows indicate the increased fluorescent signal indicating hemorrhaging. Scale bar: 100 µm. (B) Hemorrhaging at 3 dpf following static AFN exposure beginning at 6 hpf, given as the percentage of larvae with the phenotype out of the total number of larvae at each time point. (C) Images of Tg(sox10:EGFP) embryos at 4 dpf (lateral view), DMSO control is top and 0.5 µM AFN is bottom. Arrows indicate malformation of the ceratohyal (black) and Meckel's (red) facial cartilage. Scale bar: 100 µm. (D) Jaw defects at 4 dpf following static AFN exposure beginning at 6 hpf, given as the percentage of larvae with the phenotype out of the total number of larvae at each time point. The values in B and D represent the mean percentage±SEM for five biological replicates with each treatment group containing on average 40 embryos. Statistically significant differences are noted as *p≤0.05 (1 µM), and ***p≤0.001.