Extended Data Fig. 7: Effects of the fluorogens on zebrafish embryogenesis.
From: Orthogonal fluorescent chemogenetic reporters for multicolor imaging
Zebrafish embryos were incubated with 5 μM fluorogen during 1 h at 50% epiboly or overnight (ON) from 50% epiboly to 24 hpf. The graph shows the percentage of embryos with no defect (white), axis defects (grey), or dead (black) at 48 hpf. Controls untreated and treated with DMSO only were performed. The number (n) of embryos used for each condition is indicated.
