Tissue culture and rapid propagation method of traditional Chinese medicine cissus assamica
A red-backed silk, tissue culture and rapid propagation technology, applied in the field of plant tissue culture, can solve the problems that there is no red-backed silk tissue culture technology, no patent application for red-backed silk tissue culture and rapid propagation, and achieve low cost and easy operation The effect of strong performance and simple process
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[0018] Example 1
[0019] (1) Explant collection: In the field, select the middle and upper parts of the vine plants with robust growth and no obvious disease, and the knotted canes with full sun as explants, and immediately after collection, carry out water retention and moisturizing treatment and bring them back to the laboratory in time .
[0020] (2) Induction culture: when the explants collected in step (1) are collected back to the laboratory, rinse them with tap water overnight, place them on a clean bench, and disinfect them in 75% ethanol solution for 5 seconds. After 5 times of rinsing with sterile water After absorbing the water with sterile filter paper, place it in a 0.1% mercuric solution for 15 minutes of disinfection, rinse it with sterile water for 5 times, absorb the water with sterile filter paper, cut it into 1.5-2.5cm knotted canes and cut them into pieces. Inoculated into the induction medium, placed at 25°C for 45 days in total dark culture, and the for...
Example Embodiment
[0025] Embodiment 2
[0026] (1) Explant collection: In the field, select the middle and upper parts of the vine plants with robust growth and no obvious disease, and the knotted canes with full sun as explants, and immediately after collection, carry out water retention and moisturizing treatment and bring them back to the laboratory in time .
[0027] (2) Induction culture: when the explants collected in step (1) were collected back to the laboratory, rinsed with tap water overnight, placed in a clean bench, and sterilized in 75% ethanol solution for 7 seconds, and rinsed with sterile water for 6 times. After absorbing the water with sterile filter paper, it was placed in 0.1% mercuric solution for 17 minutes of disinfection. After 6 times of rinsing with sterile water, the water was absorbed with sterile filter paper, and then cut into 1.5-2.5cm knotted canes. Inoculated into the induction medium, and placed at 27°C for 47 days in the dark to induce the formation of advent...
Example Embodiment
[0032] Embodiment 3
[0033] (1) Explant collection: In the field, select the middle and upper parts of the vine plants with robust growth and no obvious disease, and the knotted canes with full sun as explants, and immediately after collection, carry out water retention and moisturizing treatment and bring them back to the laboratory in time .
[0034](2) Induction culture: when the explants collected in step (1) are collected back to the laboratory, first rinse them with tap water overnight, place them on a clean bench, and sterilize them in 75% ethanol solution for 10 seconds. After 7 times of rinsing with sterile water After absorbing the water with sterile filter paper, place it in 0.1% mercuric solution for 20 minutes for disinfection, rinse it with sterile water for 7 times, absorb the water with sterile filter paper, cut into 1.5-2.5cm knotted canes and cut them into pieces. Inoculated into the induction medium, placed at 28°C for 50 days in full dark culture, and the...
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