Tissue culture and rapid propagation technology for ulmus pumila Linn.
A technology of tissue culture rapid propagation and technology, applied in the field of plant tissue culture, can solve the problems of limited number and speed of reproduction, the tissue culture system of elm tree is not fully mature, and the difficulty of rooting cuttings, etc., to achieve the effect of rapid propagation
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Embodiment 1
[0017] (1) Collection and processing of explants: Pick the shoots in seasons when the plants grow vigorously and the temperature is relatively cool, wrap the incisions with moist absorbent cotton, and store them in a -4°C refrigerator for later use. Cut the axillary buds of the stem into about 2-3 cm long, remove the leaves and terminal buds, keep a little petiole, soak in washing powder water for 10 minutes, rinse with tap water for 1 hour after brushing, then disinfect with 75% ethanol for 5 seconds, and then wash 3 times with sterile water. Then disinfect with 0.1% mercuric chloride solution for 10 minutes, rinse with sterile water for 4 times, and absorb the water with sterile filter paper.
[0018] (2) Primary culture: Inoculate the stem segment from step (1) on the primary culture medium, culture it in total darkness at 25°C for 15 days, then place it under the condition of 12 hours of light per day, and cultivate it for 28 days at a light intensity of 1500 lx. That ...
Embodiment 2
[0023] (1) Collection and processing of explants: Pick the shoots in seasons when the plants grow vigorously and the temperature is relatively cool, wrap the incisions with moist absorbent cotton, and store them in a -4°C refrigerator for later use. Cut the axillary buds of the stem segment into about 2-3 cm long, remove the leaves and terminal buds, keep a little petiole, soak in washing powder water for 12 minutes, rinse with tap water for 2 hours after brushing, disinfect with 75% ethanol for 8 seconds, and wash 5 times with sterile water. Then sterilize with 0.1% mercuric chloride solution for 13 minutes, rinse with sterile water for 5 times, and absorb the water with sterile filter paper.
[0024] (2) Primary culture: inoculate the stem segment from step (1) on the primary culture medium, culture it in total darkness at 27°C for 17 days, then place it in the light for 14 hours a day, and cultivate it for 26 days at a light intensity of 2000 lx. That is to induce the f...
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