Establishing method of scrophularia ningpoensis tissue culture system
An establishment method and tissue culture technology, applied in the field of establishment of Scrophularia scrophulariae tissue culture system, can solve the problems of reduced survival rate and seedling rate, low germination rate, high cost, etc., and achieve improved propagation speed and scale, simple process method, The effect of easy operation
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Embodiment 1
[0016] (1) Disinfection of explants: Rinse the collected stems with clean water for 15 minutes and gently brush off the impurities on them with a brush. Disinfect them in 75% ethanol solution for 15 seconds in an ultra-clean workbench, and then wash them with sterile water for 8 seconds. Rinse with 5% Antifoam solution for 8 minutes, rinse with sterile water for 8 times, and then use sterile filter paper to absorb the water and set it aside.
[0017] (2) Induction culture: cut the sterilized stems in step (1) into about 6 cm long stems according to the paired buds as a unit, cut off the browned part of the bottom of the stems during the treatment, and inoculate them into the induction medium Bud induction culture was carried out. After inoculation, they were first cultured in total darkness at 26°C for 6 days, and then illuminated for 15 hours a day with a light intensity of 3000lx. They were cultured at a temperature of 26°C until adventitious buds formed, and the induction r...
Embodiment 2
[0022] (1) Disinfection of explants: Rinse the collected stems with clean water for 12 minutes and gently brush off the impurities on them with a brush. Disinfect them with 75% ethanol solution in an ultra-clean workbench for 25 seconds, and then wash them with sterile water for 8 seconds. Rinse again with 6% Antifoam solution for 10 minutes, rinse with sterile water for 8 times, and then use sterile filter paper to absorb the water before use.
[0023] (2) Induction culture: Cut the sterilized stems in step (1) into about 8 cm long stems according to the paired buds as a unit, cut off the browned part of the bottom of the stems during the treatment, and inoculate them into the induction medium Bud induction culture was carried out. After inoculation, they were first cultured in total darkness at 29°C for 6 days, and then illuminated for 15 hours a day with a light intensity of 3000lx and a culture temperature of 29°C until adventitious buds formed, and the induction rate was ...
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