Method for cultivating aseptic seedling of Ferula sinkiangensis
A cultivation method and technology for sterile seedlings, applied in germination equipment, seed immunization, seed and rhizome treatment, etc., can solve the problems of inability to form large-scale, harsh growth environment, and reduced success rate of cell culture, so as to maintain biodiversity. , Improve the success rate of training and protect the effect of drug resources
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Embodiment 1
[0018] Select clean, plump, and consistent seeds, immerse the selected seeds in 70% alcohol for 25 seconds, drain until there is no dripping, and then place them in 10% H2O by volume. 2 o 2 Soak in the solution for 15 minutes, drain until there is no drip, rinse with sterile water, and drain until there is no drip. After draining until there is no drip, rinse twice with sterile water twice the weight of the seed, and drain until there is no drip. The germination bed is a sand bed, and the sand bed is first cooled to 4-10°C, the detoxified seeds are placed on the seed germination bed, and cultivated at 4°C for 30 days. During the germination period, observe and record the germination situation at any time. When the radicle breaks through more than 1 / 2 of the length of the seed, it can be As a material for tissue culture, seedling planting or transplanting in the next step.
Embodiment 2
[0020] Select clean, plump, and consistent seeds, immerse the selected seeds in 50% alcohol for 35 seconds, drain until there is no dripping phenomenon, and then place them in H2O with a concentration of 15% by volume. 2 o 2 Soak in the solution for 10 minutes, drain until there is no dripping phenomenon, rinse with 5 times the weight of sterile water 3, drain until there is no dripping, spread the sterilized seeds on the sterile germination bed on the fully sterilized sand bed , the thickness should be such that there is no upper and lower overlap between the seeds. Keep the relative humidity of the environment at 55%, and cultivate it at a temperature of 10°C for 60 days. During the germination period, observe and record the germination situation. When more than 70% of the seed radicle breaks through more than 1 / 2 of the seed The resulting germ can be used as a material for tissue culture, seedling planting or transplanting and cutting in the next step.
Embodiment 3
[0022] Select clean, plump, and consistent seeds, immerse the selected seeds in 60% alcohol for 30 seconds, drain until there is no dripping, and then put them in H2O with a volume percentage concentration of 14%. 2 o 2 Soak in the solution for 14 minutes, drain until there is no drip, rinse with sterile water, and drain until there is no drip. Rinse twice with sterile water 3 times the weight of the seeds until there is no dripping, and drain until there is no dripping. The germination bed is a sand bed, and the sand bed is first sterilized by ultraviolet rays for 60 minutes, and the seeds after decontamination Place it on the seed germination bed and culture it at 7°C for 30 days. During the germination period, observe and record the germination situation at any time. When the radicle of more than half of the seeds breaks through more than 1 / 2 of the length of the seeds, it can be used as the next step Materials for tissue culture, seedling planting or transplanting, etc. ...
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