Figure 3
Figure 3. In vivo enhancer assay using EGFP reporter constructs in zebrafish embryos. (A) Representative mosaic G0 animals, at 5 dpf, for 5 EGFP reporter constructs (CNC4, CNC10, CNC12, and CNC13) as well as for the control plasmid carrying no CNC sequences (Control). The 2-bottom pictures are higher magnification of the areas defined by dashed line of Control and CNC12 constructs, the last one driving EGFP expression in liver (white arrow). (B) CNC12-EGFP and control transgenic representative G1 animals at 5 dpf. Higher magnification of an 8-dpf CNC12-EGFP transgenic individual depicts clear liver expression of the reporter gene. Embryos are shown in lateral view, anterior to the right in all panels.

In vivo enhancer assay using EGFP reporter constructs in zebrafish embryos. (A) Representative mosaic G0 animals, at 5 dpf, for 5 EGFP reporter constructs (CNC4, CNC10, CNC12, and CNC13) as well as for the control plasmid carrying no CNC sequences (Control). The 2-bottom pictures are higher magnification of the areas defined by dashed line of Control and CNC12 constructs, the last one driving EGFP expression in liver (white arrow). (B) CNC12-EGFP and control transgenic representative G1 animals at 5 dpf. Higher magnification of an 8-dpf CNC12-EGFP transgenic individual depicts clear liver expression of the reporter gene. Embryos are shown in lateral view, anterior to the right in all panels.

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