Tissue culture and rapid propagation method for dracaena cochinchinensis
A technology of dragon blood tree and tissue culture, applied in the field of plant reproduction, can solve the problems of difficulty in realizing large-scale cultivation, limited number of seedlings, low reproduction rate, etc., and achieves improvement of seedling quality, reduction of cost consumption and cost reduction. Effect
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Embodiment 1
[0023] An example of the method for rapid propagation of the tissue culture of Dracaena in the present invention includes the following steps:
[0024] (1) Selection and disinfection of explants: Take dracaena seeds as explants, soak them in a 2% detergent solution for 5 minutes, rinse with linear tap water for 15-30 minutes, and add 2-3 drops of Tween. -20 100 ml 0.1% mercury disinfection for 8-10 minutes, rinse with sterile water for 3-5 times, and finally remove the surface moisture with sterile filter paper to obtain explants, wherein the sterile water is autoclaved distilled water;
[0025] (2) Seed germination to obtain sterile test tube seedlings: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500 lux, and light time of 12-14 hours / day Cultivate for 30 days under the conditions of, and obtain sterile test tube seedlings after germination. MS medium contains 1.0 mg / L 6-benzyl adenine 6-BA, 0.2 mg / L indole ac...
Embodiment 2
[0031] Another example of the tissue culture rapid propagation method of Dracaena vulgaris according to the present invention includes the following steps:
[0032] (1) Selection and disinfection of explants: Take dracaena seeds as explants, soak them in a 2% detergent solution for 5 minutes, rinse with linear tap water for 15-30 minutes, and add 2-3 drops of Tween. -20 100 ml 0.1% mercury disinfection for 8-10 minutes, rinse with sterile water for 3-5 times, and finally remove the surface moisture with sterile filter paper to obtain explants, wherein the sterile water is autoclaved distilled water;
[0033] (2) Seed germination to obtain sterile test tube seedlings: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500 lux, and light time of 12-14 hours / day Cultivate for 30 days under the conditions of, and obtain sterile test tube seedlings after germination. MS medium contains 1.0 mg / L 6-benzyl adenine 6-BA, 0.2 m...
Embodiment 3
[0039] Another example of the tissue culture rapid propagation method of Dracaena vulgaris according to the present invention includes the following steps:
[0040] (1) Selection and disinfection of explants: Take dracaena seeds as explants, soak them in a 2% detergent solution for 5 minutes, rinse with linear tap water for 15-30 minutes, and add 2-3 drops of Tween. -20 100 ml 0.1% mercury disinfection for 8-10 minutes, rinse with sterile water for 3-5 times, and finally remove the surface moisture with sterile filter paper to obtain explants, wherein the sterile water is autoclaved distilled water;
[0041] (2) Seed germination to obtain sterile test tube seedlings: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500 lux, and light time of 12-14 hours / day Cultivate for 30 days under the conditions of, and obtain sterile test tube seedlings after germination. MS medium contains 1.0 mg / L 6-benzyl adenine 6-BA, 0.2 m...
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