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Figure Caption
Fig. S12
Set-up for time-lapse imaging of zebrafish lens epithelium
(A) Schematic illustration of the imaging setup.
(B) Real set-up picture.
(C) The embryo was mounted in 1% low-melting agarose, and the yolk was put into the groove in order to orient the embryo laterally.
(D) The agarose was restricted within the inner circle of a strengthening ring on the groove stretched into the acrylic plate.
(E) The lateral side of the embryonic eye was used for confocal z-stack scanning.
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