Fig. 3

Fig. 3

a, Images of a zebrafish larvae (roughly 30 hpf, nuclei labeled with tg(h2afva:h2afva-mCherry) imaged using the microscope. Imaging volume (x,y,z) is 3,000 × 800 × 300 μm acquired every 50 s (two views). The depth is color-coded, where blue and red indicate respectively close to and far from the coverglass. Scale bar, 100 μm. b, Four xy slices from different regions (1–4, dashed squares in a) at various depths and one xz slice (5, dashed line in a) are highlighted. Scale bar, 50 μm. c, Images of Drosophila fly egg chambers. Nuclei of germline cells (large) and somatic cells (small) were labeled by expressing UAS-NLS-GFP under the control of Usp10-Gal4 (BDSC-76169). Imaging volume is 3,000 × 800 × 180 μm acquired every 30 s (single views) for 3 h. The depth is color-coded as above. Scale bar, 100 μm. d, Four regions (dashed squares in c) are highlighted. Scale bar, 50 μm.