Sophora flavescens regeneration system establishing technology
A technology of Sophora flavescens and system, applied in the field of establishment of Sophora flavescens regeneration system, can solve the problems of long growth cycle and low reproduction coefficient, and achieve the effect of solving the high difficulty of introduction and domestication
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Embodiment 1
[0016] (1) Disinfection of explants: Collect the delicate leaves of healthy plants of Sophora flavescens, gently scrub them with a soft brush dipped in washing powder water, rinse them with tap water for 1 hour, then place them in an ultra-clean workbench, first disinfect them with 75% ethanol for 10 seconds, and then use sterile Wash 4 times with water, then disinfect with 0.1% mercuric chloride solution for 6 minutes, rinse with sterile water 6 times, and then dry the water drops on the surface with sterile filter paper before use.
[0017] (2) Differentiation culture: Excise the petiole of the leaf treated in step (1), lightly scratch a few times on the leaf with a sterile scalpel, and inoculate the differentiation medium in such a way that the back of the leaf is in contact with the medium for callus Tissue and cluster bud induction. After inoculation, culture in total darkness at 26°C for 18 days, then light for 15 hours a day, the light intensity is 3100lx, and the cultu...
Embodiment 2
[0022] (1) Disinfection of explants: Collect the delicate leaves of healthy plants of Sophora flavescens, gently scrub with a soft brush dipped in washing powder water, rinse with tap water for 2 hours, and then place them in an ultra-clean workbench. Disinfect them with 75% ethanol for 8 seconds and then use sterile Wash 4 times with water, then sterilize with 0.3% mercury liter solution for 6 minutes, rinse 4 times with sterile water, and then dry the water droplets on the surface with sterile filter paper before use.
[0023] (2) Differentiation culture: Excise the petiole of the leaf treated in step (1), lightly scratch a few times on the leaf with a sterile scalpel, and inoculate the differentiation medium in such a way that the back of the leaf is in contact with the medium for callus Tissue and cluster bud induction. After inoculation, culture in total darkness at 26°C for 24 days, then light for 14 hours a day, the light intensity is 3400lx, and the culture temperature...
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