A slicing method suitable for observing the anatomical structure of rubber tree flowers
An anatomical structure, rubber tree technology, applied in the direction of instruments, scientific instruments, test sample preparation, etc., can solve the problems that flower organs are easily corroded and dissolved, it is difficult to observe the complete structure, and the quality of slices is not easy to repeat, etc. Achieve repeatability and versatility Batch screening, good repeatability and versatility, and convenient material collection
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Embodiment 1
[0055] Embodiment 1, the anatomical structure observation of rubber tree female flower, male flower and flower stalk
[0056] In this example, the anatomical structure of the flower organs was observed by using the spring flowers of the 9-year-old tree of the rubber tree variety CATAS 7-33-97.
[0057] Experimental conditions: In April, the inflorescences of the 9-year-old inflorescence of the rubber tree clone variety CATAS 7-33-97 were collected, and the female flowers, male flowers and flower stalks were collected respectively. The trimming method is as follows:
[0058] 1) Female flower: Pick the female flower at the top of the inflorescence and the ovary begins to develop, cut off the flower stalk with a single-sided blade, and cut off the epidermis of 0.2cm×0.2cm on the side of the enlarged ovary to form a small opening, such as figure 1 As shown, the dotted line shows the part of trimming the ovary of the female flower;
[0059] 2) Unopened male flowers: Pick the matu...
Embodiment 2
[0069] Same as Example 1, except for the following differences: the female flower incision is 0.1 cm x 0.1 cm, the unopened male flower incision is 0.1 cm x 0.3 cm, and the flower stalk is cut in lengths of 0.3 cm and 0.8 cm.
Embodiment 3
[0071] Same as Example 1, except for the following differences: the fixative is 2wt% paraformaldehyde and 5wt% glutaraldehyde in 0.01M phosphate buffer, pH 7.2; the first wash process is 0.005M phosphate buffer, pH 7.8 , the soaking time is 10min; the second time is a mixed solution of two-thirds of 0.005M pH 7.8 phosphate buffer and one-third of the OCT embedding medium, the soaking time is 20min; the third time is the OCT embedding medium , soaking time 40min.
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