Method for establishing radix stellariae tissue culture systems
An establishment method and technology of Yin Bupleurum, applied in the establishment field of Yin Bupleurum tissue culture system, can solve the problems of reducing survival rate and seedling rate, low income and high cost, and achieve the improvement of reproduction speed and scale, high seed reproduction coefficient, Realize the effect of factory production
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Embodiment 1
[0016] (1) Disinfection of explants: Rinse the collected stems of Bupleurum chinensis with clear water for 5 minutes and gently brush off the impurities on them with a brush. Disinfect them with 75% ethanol solution in an ultra-clean workbench for 5 seconds, and then use non-toxic Bacterial water was washed 6 times, and then rinsed with 5% Antifoam solution for 7 minutes, rinsed with sterile water 6 times, and then used sterile filter paper to absorb the water before use.
[0017] (2) Induction culture: Cut the stems of Silver Bupleurum sterilized in step (1) into about 2.0 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 into Bud induction culture was carried out in induction medium. After inoculation, they were first cultured in total darkness at 26°C for 5 days, and then placed in light for 10 hours a day with a light intensity of 2100lx, and placed at a culture temperature of 25°C ...
Embodiment 2
[0022] (1) Disinfection of explants: Rinse the collected stems of Bupleurum chinensis with clear water for 8 minutes and gently brush off the impurities on them with a brush. Disinfect them with 75% ethanol solution in an ultra-clean workbench for 16 seconds. Bacteria washed twice, then rinsed with 5% Antifoam solution for 4 minutes, rinsed twice with sterile water, and then blotted with sterile filter paper for later use.
[0023] (2) Induction culture: Cut the stems of Silver Bupleurum sterilized in step (1) into about 1.0 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 into Bud induction culture was carried out in induction medium. After inoculation, they were first cultured in total darkness at 26°C for 2 days, and then placed in light for 9 hours a day with a light intensity of 2400lx, and cultured at a temperature of 26°C until adventitious buds formed, and the induction rate wa...
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