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Fig. S1 Illumination by the confocal microscope laser is inefficient in causing apoptosis. (A-E) Changes in fluorescence intensity of SqKR2 embryo during 80 minutes of continuous confocal imaging. (F-K) Illumination by green light of mercury lamp in the widefield mode increases apoptosis in the hindbrain of the SqKR2 embryo (G, J). Relatively few apoptotic cells in the SqKR2 embryo were detected following continuous confocal imaging (H, K). The otic vesicle is defined by yellow broken line (Figure 2F-H).
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Full text @ BMC Dev. Biol.