Manufacturing method of paraffin section of hermatypic coral oocyte
An oocyte and paraffin section technology, which is applied in the preparation of test samples and other directions, can solve the problems affecting the prediction of the ovulation time of reef-building corals, the difficulty of underwater operation, and the inaccurate ovulation time of reef-building corals.
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[0024] (1) The healthy staghorn coral fragments containing reef-building coral oocytes were collected from the bottom of the Luhuitou Peninsula. The diameter of the individual staghorn corals was greater than 20 cm. The samples were collected from January to May 2007;
[0025] (2) Fix the collected staghorn coral containing oocytes with 4% seawater formaldehyde solution for 24 hours;
[0026] (3) Use pure water to wash away the residual seawater formaldehyde solution, and then use 50% formic acid solution to remove the calcareous skeleton of reef-building corals for 36 hours;
[0027] (4) To remove the water in the tissue, use ethanol to dehydrate in the order from low concentration to high concentration, followed by 50% ethanol, 70% ethanol, 80% ethanol, 90% ethanol, 95% ethanol and absolute ethanol, 2 hours each time; (5) To clear the tissue, immerse the tissue in a 1:1 ethanol-xylene premix for 1.5 hours, and then immerse the tissue in 100% xylene for 30 minutes. ;
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