Tissue culture method for improving multiplication coefficient of catalpa bungei and special culture medium
A technology of proliferation coefficient and tissue culture, which is applied to the tissue culture of catalpa tree, the tissue culture method for improving the multiplication coefficient of catalpa tree and the field of special medium, which can solve the problems of long growth cycle, cumbersome steps, low proliferation rate, etc. The effect of promoting the proliferation of axillary buds with simple steps and great application prospects
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Embodiment 1
[0031] Embodiment 1 improves the tissue culture method of catalpa multiplication coefficient
[0032] (1) Select the stem section or terminal bud of the old Catalpa tree with axillary buds cut to a length of 10 cm, cut off the leaves and keep the petiole of 1.5 cm, soak in detergent for 10 minutes, and then rinse under running water for 20 minutes; On the workbench, soak with 75% alcohol for 30s, then treat with 0.1% mercury liter for 5 minutes, rinse with sterile water for 4 times, cut the petiole to 3mm again to avoid residue, inoculate into the primary culture medium, each bottle The medium is inoculated with 2-3 stem segments, and the first generation is cultured for at least 28 days to obtain the first generation of sterile seedlings;
[0033] Wherein, the formula of the first-generation medium is: MS medium+6-BA 0.5mg / L+IAA 0.15mg / L, the condition of the first-generation culture is aseptic culture at a temperature of 25°C, the light time is 16h / d, and the light intensity...
Embodiment 2
[0037] The test material is "Luqi No. 1".
[0038] (1) Selection of explants: In the experimental nursery of Shandong Provincial Academy of Forestry, cut the young shoots of the old catalpa tree (No. Branch work should be carried out on sunny days.
[0039] (2) Sterilization of explants: cut off the leaves on the tender stems and keep the petioles of 1-2 cm, soak and clean the stems with detergent for 5-10 minutes, and then rinse them under running water. On the ultra-clean workbench, soak in 75% alcohol for 30 seconds, then soak in 0.1% mercury chloride for 5-8 minutes, and then wash with sterile water for 3-4 times. Cut the petiole to 3-5mm again to avoid residue.
[0040] (3) Cultivation of sterile seedlings: cut the sterilized explants into about 1.5cm long stems with axillary buds, and insert them into the primary medium of MS+6-BA0.5mg / L+IAA0.15mg / L 2-3 stem segments were inoculated in each bottle, and the primary culture conditions were aseptic culture at a temperatu...
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