A kind of tissue culture rapid propagation method of seedling medicine Teng
A technology of tissue culture and rapid propagation of A. japonica, which is applied in the field of plant tissue culture, can solve the problems of no patent application for tissue culture and rapid propagation of s. , low cost, strong technical effect
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Embodiment 1
[0020] (1) Explant collection: In the wild, select the middle and upper part of the plant of the black bone vine with no obvious diseases, and the sunny and substantial cane with joints as explants. After collection, water retention and moisturizing treatment should be carried out immediately and brought back to the laboratory in time. .
[0021] (2) Explant induction: when step (1) is collected back to the laboratory, the explants are first rinsed under tap water overnight, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 15 seconds, rinsed with sterile water for 5 seconds After the first time, dry the water with sterile filter paper, sterilize it in 0.1% mercuric chloride solution for 15 minutes, wash it with sterile water for 5 times, dry it with sterile filter paper, and cut it into 1.5-2.5cm vines with knots. The stems are inoculated into the induction medium, placed at 25° C. for 30 days in full dark culture to induce the formation of adventi...
Embodiment 2
[0027] (1) Explant collection: In the wild, select the middle and upper part of the plant of the black bone vine with no obvious diseases, and the sunny and substantial cane with joints as explants. After collection, water retention and moisturizing treatment should be carried out immediately and brought back to the laboratory in time. .
[0028] (2) Explant induction: when step (1) is collected back to the laboratory, the explants are first rinsed under tap water overnight, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 17 seconds, rinsed with sterile water for 6 After the first time, dry the water with sterile filter paper, sterilize it in 0.1% mercuric chloride solution for 18 minutes, wash it with sterile water for 6 times, dry it with sterile filter paper, and cut it into 1.5-2.5cm vines with knots. The stems are inoculated into the induction medium, placed at 27°C for 33 days in full dark culture to induce the formation of adventitious buds...
Embodiment 3
[0034] (1) Explant collection: In the wild, select the middle and upper part of the plant of the black bone vine with no obvious diseases, and the sunny and substantial cane with joints as explants. After collection, water retention and moisturizing treatment should be carried out immediately and brought back to the laboratory in time. .
[0035](2) Explant induction: when step (1) is collected back to the laboratory, the explants are first rinsed under tap water overnight, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 20 seconds, rinsed with sterile water for 7 After the first time, dry the water with sterile filter paper, sterilize it in 0.1% mercuric chloride solution for 20 minutes, wash it with sterile water for 7 times, dry it with sterile filter paper, and cut it into 1.5-2.5cm vines with knots. The stems are inoculated into the induction medium, placed at 28° C. for 35 days in full dark culture to induce the formation of adventitious bud...
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