Intermediate propagation method of vernonia amygdalina
A fast technology of Vernonia almond, applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve the problems of difficult cleaning of the culture medium, degradation of breeding seedlings, lower survival rate, etc., so as to overcome the degradation of breeding seedlings and reduce the Diseases, the effect of reducing the survival rate
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Embodiment 1
[0031] Propagate Almond Vernonia by following these steps:
[0032] (1) Induction of explants: Stems were cut from Vernonia amygdala plants, which were growing robustly and free from diseases and insect pests, as explants, soaked in a diluted solution of detergent, and then cleaned the surface of the explants with a brush. Then rinse with running water for about 1 hour, soak in alcohol with a volume ratio of 75% for about 25 seconds on the ultra-clean workbench, rinse with sterile water for 3 times, then disinfect with 1g / L mercury chloride solution for about 9 minutes, rinse with sterile water After 3 times, inoculate in MS starting medium containing 1mg / L6-BA and 0.1mg / LNAA, culture temperature is 25°C, light intensity is 1500LX, light time is 13h per day;
[0033] (2) Subculture of induced buds: when the induced buds grow to 2~3cm, inoculate them into MS proliferation medium containing 1mg / L6-BA and 0.1mg / LNAA, the temperature is 25℃, the light intensity is 1500LX, and the ...
Embodiment 2
[0039] Propagate Almond Vernonia by following these steps:
[0040] (1) Induction of explants: Stems were cut from Vernonia amygdala plants, which were growing robustly and free from diseases and insect pests, as explants, soaked in a diluted solution of detergent, and then cleaned the surface of the explants with a brush. Then rinse with running water for 0.5h, soak in alcohol with a volume ratio of 75% for 20s on the ultra-clean workbench, rinse with sterile water twice, then disinfect with 1g / L mercury chloride solution for 10min, rinse with sterile water twice Afterwards, inoculate in the MS starting medium containing 0.5mg / L6-BA and 0.05mg / LNAA, the culture temperature is 23°C, the light intensity is 2000LX, and the light time is 10h per day;
[0041] (2) Subculture of induced buds: when the induced buds grow to 2~3cm, inoculate them into MS proliferation medium containing 0.5mg / L6-BA and 0.05mg / LNAA, the temperature is 23°C, and the light intensity is 2000LX. The light ...
Embodiment 3
[0047] Propagate Almond Vernonia by following these steps:
[0048] (1) Induction of explants: Stems were cut from Vernonia amygdala plants, which were growing robustly and free from diseases and insect pests, as explants, soaked in a diluted solution of detergent, and then cleaned the surface of the explants with a brush. Then rinse with running water for 0.8h, soak in alcohol with a volume ratio of 75% for 30s on the ultra-clean workbench, rinse with sterile water for 4 times, then disinfect with 1g / L mercury chloride solution for 8min, and rinse with sterile water for 4 times Afterwards, inoculate in the MS starting medium containing 1mg / L6-BA and 0.05mg / LNAA, the culture temperature is 28°C, the light intensity is 1500~2000LX, and the light time is 15h per day;
[0049] (2) Subculture of induced buds: when the induced buds grow to 2~3cm, they are inoculated into MS proliferation medium containing 0.5mg / L6-BA and 0.1mg / LNAA, the temperature is 28℃, and the light intensity i...
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