Method for cultivating and breeding cell tissue of tissue culture seedling of Dendrobium candidum
A technology of dendrobium candidum and cell tissue, applied in the field of cell tissue culture and breeding of dendrobium candidum tissue culture seedlings, can solve the problems of unfavorable preservation of good varieties, separation of characters, etc.
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Embodiment 1
[0031] The Dendrobium officinale plant is cleaned with pure water, the leaves are removed, and the outer sheath of the plant is peeled off with tweezers. Soak the plants in 0.1% mercuric chloride solution for disinfection for 15 minutes on the ultra-clean workbench in the clean room. After disinfection, the plants were taken out, rinsed with sterile water, and cut into sections with a sterile scalpel, each section 2.5 cm long. The plant segments were inoculated on the callus culture medium, and cultured at a temperature of 23° C., a humidity of 35%, an illumination of 1800 Lx, and 10 hours of illumination per day. The culture time was 70 days, and the callus grew out. Cut off the callus with a sterile scalpel on an ultra-clean workbench, crush and disperse it with sterile tweezers. The crushed callus was put into the cell culture medium and placed on a shaker for normal temperature culture for 15 days. At the end of the shaker culture, the cells proliferated in the cell cul...
Embodiment 2
[0046] The Dendrobium officinale plant is cleaned with pure water, the leaves are removed, and the outer sheath of the plant is peeled off with tweezers. Soak the plants in 0.1% mercuric chloride solution for disinfection for 15 minutes on the ultra-clean workbench in the clean room. After disinfection, the plants were taken out, rinsed with sterile water, and cut into sections with a sterile scalpel, each section 3.0 cm long. The plant segments were inoculated on the callus culture medium, and cultured at a temperature of 25° C., a humidity of 40%, an illumination of 1800 Lx, and 10 hours of illumination per day. The culture time was 65 days, and the callus grew out. Cut off the callus with a sterile scalpel on an ultra-clean workbench, crush and disperse it with sterile tweezers. The crushed callus was put into the cell culture medium and placed on a shaker for normal temperature culture for 20 days. At the end of the shaker culture, the cells proliferated in the cell cul...
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