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. 2020 Mar 24;30(12):4292–4302.e7. doi: 10.1016/j.celrep.2020.03.024

Figure 2.

Figure 2

Pectoral Fin Growth

(A–F) Scanning electron micrographs of larvae (A–C) and fins (D–F) at different times. Cartoon indicates fin orientation.

(G–I) DAPI (blue) and Phospho-histoneH3 immunostainings (red) at different times.

(J–L) Overlay of fins expressing zGeminin. LUT shows number of overlaid zGeminin+ nuclei per pixel. Dashed line, fin boundary. Distal, down; anterior, left.

(M) PD and AP fin lengths from SEM images.

(N) Number of phospho-histoneH3 cells per 10,000 μm2 at different times. Line, exponential fit with goodness of fit (R2).

(O) Log-log plot of AP versus PD lengths to determine anisotropy ε (slope value) ± SEM. Line, power-law fit with goodness of fit (R2).

Black dots, average from developmental time bins. Mean ± SEM are shown in all graphs. n represents total number of fins analyzed/overlaid. Scale bars, 100 μm (A–C), 50 μm (D–L).