Microscopy from Scientific Research

Confocal micrographs (A and C) and boxplots (B and D) showing E-cadherin fluorescence intensity in a.u. at 1 and 18 hpi. (A)–(D) show the changes in junctional E-cadherin under HU treatment (A and B) andNp63MO (C and D). Quantification and statistical analyses were performed usingn= the total number of cells collected from multiple embryos, as indicated below graphs (e, embryos; c, cells). Scale bars: 25 m (A and C) Calibration bars: 0–1,500 a.u. (A) and 0–1,250 a.u. (C). hpi, hours post-injection

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