Tissue culture reproduction method of Chinese evergreen
A technology of tissue culture and induction medium, which is applied in the field of tissue culture and propagation of Sclerostifolia, can solve the problems such as no tissue culture of Scleracea, and achieve the effect of accelerating the propagation speed, maintaining excellent traits, and high stability
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Embodiment 1
[0024] a. Material selection: Select young stems of Aglaonema rotundum as explants during the growing season.
[0025] b. Disinfection of explants and induction of adventitious buds: Rinse the young stems of R. rotundum under tap water, soak them for 30 seconds in 70% alcohol by volume fraction, and then use mass volume percentage concentration Disinfect with 0.1% mercuric chloride solution for 8 minutes, rinse with sterile water 4 times, cut into segments about 1 cm long, inoculate them on the induction medium, take out the segments after 5 days and use 0.1% mercuric chloride in mass percent concentration again The solution was sterilized for 8 minutes, rinsed with sterile water for 5 times, and then transferred to a new induction medium. The success rate of disinfection was 71%, and adventitious buds could be formed on the explants in 60 days. Contains 2.0mg of 6-benzylpurine, 0.2mg of naphthaleneacetic acid, 20g of sucrose, 6g of agar, and the rest are MS;
[0026] c. Subc...
Embodiment 2
[0033] a. Material selection: Select young stems of Aglaonema Silver King as explants during the growing season.
[0034] b. Disinfection of explants and induction of adventitious buds: Rinse the young stems of Grasshopper spp. under tap water, soak them in 75% alcohol for 45 seconds, and then sterilize them with 0.15% mercuric chloride solution for 10 minutes , washed 5 times with sterile water, cut into 1 cm-long segments, inoculated on the induction medium, took out the segments after 6 days, sterilized with 0.15% mercuric chloride solution for 8 minutes, rinsed with sterile water 5 times, and then In the new induction medium, the disinfection success rate can reach 78%, and adventitious buds can be formed on the explants in 60 days. The induction medium contains 3.0 mg of 6-benzylpurine and 0.5 mg of naphthaleneacetic acid per liter. milligrams, 25 grams of sucrose, 7 grams of agar, and the rest are MS;
[0035] c. Subculture proliferation: the induced adventitious buds a...
Embodiment 3
[0042] a. Material selection: select young stems of Aglaonema Tembaga Super Red as explants during the growing season.
[0043] b. Disinfection of explants and induction of adventitious buds: Rinse the young stems of Sclerophyllum superrhiza under tap water, soak them in 80% alcohol for 60 seconds, and then sterilize them with 0.2% mercuric chloride solution for 8 minutes , washed 5 times with sterile water, cut into segments about 1 cm long, inoculated on the induction medium, took out the segments after 7 days, sterilized again with 0.1% mercuric chloride solution for 8 minutes, rinsed with sterile water 5 times, and then In the new induction medium, the disinfection success rate can reach 79%, and adventitious buds can be formed on the explants in 50 days. The induction medium contains 5.0 mg of 6-benzylpurine and 1.0 mg of naphthaleneacetic acid per liter. milligrams, 30 grams of sucrose, 7 grams of agar, and the rest are MS;
[0044] c. Subculture proliferation: the indu...
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