Tissue-culture and rapid-propagation method for traditional Chinese medicine capparis versicolor
A technique for tissue culture and rapid propagation of chickens, which is applied in the field of tissue culture and rapid propagation of traditional Chinese medicine chickens, can solve problems such as the absence of chickens and the application of patents for tissue culture and rapid propagation of chickens, and achieves Low cost, promotion of plant resources development, high reproduction coefficient effect
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Embodiment 1
[0019] (1) Collection of explants: In Bobai County, Guangxi, the middle and upper segmented stems of the vigorously growing Qutou chicken plants without obvious diseases are selected as explants, and the explants are immediately treated with water retention and moisturizing and brought back in time laboratory.
[0020] (2) Explant induction: The explants collected in step (1) and returned to the laboratory were rinsed under tap water for 4 hours, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 20 seconds, sterile water Rinse 5 times, blot dry with sterile filter paper, sterilize in 0.1% mercuric chloride solution for 20 minutes, rinse 8 times with sterile water, blot dry with sterile filter paper, cut into 2.0-2.5cm strips The nodal stem segments are inoculated into the induction medium, placed at 25° C. for 30 days in full dark culture to induce the formation of adventitious buds, the induction rate reaches 95%, and the pollution rate is lower th...
Embodiment 2
[0026] (1) Collection of explants: The explants were selected from Luchuan County, Guangxi Province, which grew vigorously and vigorously with no obvious diseases, and the mid-upper section of the stem with joints in the sun. After collection, it was immediately treated with water retention and moisturizing and brought back to the laboratory in time. .
[0027] (2) Explant induction: the explants collected in step (1) and returned to the laboratory were rinsed under tap water for 4 hours, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 18 seconds, sterile water Rinse 5 times, blot dry with sterile filter paper, sterilize in 0.1% mercuric chloride solution for 18 minutes, rinse 7 times with sterile water, blot dry with sterile filter paper, cut into 2.0-2.5cm strips The nodal stem segments are inoculated into the induction medium, placed at 27° C. for 32 days in full dark culture to induce the formation of adventitious buds, the induction rate reac...
Embodiment 3
[0033] (1) Collection of explants: Yangjiang County, Guangdong Province selects the middle and upper part of the stem with no obvious disease and is full of sunny and full stems of the vigorously growing Qutou chicken plant as the explants. Immediately after collection, water retention and moisturizing treatment are carried out and brought back to the laboratory in time. .
[0034](2) Explant induction: The explants collected in step (1) and returned to the laboratory were rinsed under tap water for 4 hours, placed in an ultra-clean workbench and sterilized in 75% ethanol solution for 15 seconds, sterile water Rinse 5 times, blot dry with sterile filter paper, sterilize in 0.1% mercuric chloride solution for 15 minutes, rinse 5 times with sterile water, blot dry with sterile filter paper, cut into 2.0-2.5cm strips The nodal stem segments are inoculated into the induction medium, placed at 28° C. for 35 days in full dark culture to induce the formation of adventitious buds, the...
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