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. 2020 Apr 6;147(7):dev183186. doi: 10.1242/dev.183186

Fig. 6.

Fig. 6. Localization of APR-1. (A) Localization of APR-1::GFP (vbaIs34, in white) in the SMDD/AIY mother cell during interphase. The perimeter of the SMDD/AIY mother cell (identified with ttx-3p::mCherry, otIs181) is indicated in yellow. Ventral view. Scale bar: 5 µm. (B) APR-1::GFP fluorescence intensity profile at the cortex of the cell. The x-axis provides the position at the circumference of the cell with the anterior pole in the middle and posterior pole at both ends. The grey curves represent individual cells and the red curve represents the mean curve. Top left: measure in the SMDD/AIY mother during interphase (n=11 cells analysed). Top right and bottom: the same cells were analysed during mitosis and after cytokinesis; the signal in the mother and the two daughter cells was normalized to the mean signal of the mother (n=10 divisions).

Localization of APR-1. (A) Localization of APR-1::GFP (vbaIs34, in white) in the SMDD/AIY mother cell during interphase. The perimeter of the SMDD/AIY mother cell (identified with ttx-3p::mCherry, otIs181) is indicated in yellow. Ventral view. Scale bar: 5 µm. (B) APR-1::GFP fluorescence intensity profile at the cortex of the cell. The x-axis provides the position at the circumference of the cell with the anterior pole in the middle and posterior pole at both ends. The grey curves represent individual cells and the red curve represents the mean curve. Top left: measure in the SMDD/AIY mother during interphase (n=11 cells analysed). Top right and bottom: the same cells were analysed during mitosis and after cytokinesis; the signal in the mother and the two daughter cells was normalized to the mean signal of the mother (n=10 divisions).