A kind of epimedium korean tissue culture rapid propagation method
The invention provides a rapid and rapid technology for the production of Epimedium, which can be applied in the field of Epimedium breeding, can solve the problems of difficult tissue culture of Epimedium korea, high contamination rate of explants, and there is no research on the rapid propagation of Epimedium korea, and achieves a reliable technical approach. , the stability of genetic traits, the effect of improving the quality and yield of medicinal materials
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Embodiment 1
[0035] A kind of Epimedium Korean tissue culture rapid propagation method, comprises the steps:
[0036] (1) Selection and disinfection of explants: In the late April of spring, wild rhizomes of Epimedium korean were taken, with complete overwintering buds, and the overwintering buds were full, and the tiller buds at the root were used as explants, and first rinsed under running water for 3 hours. Clean the surface appendages with washing powder, wash them twice with sterile water on an ultra-clean workbench, disinfect the surface with 75% ethanol for 30 seconds, and then rinse them with sterile water for 5 times; then disinfect with 0.1% mercury chloride for 2 minutes, and use sterile Rinse with water 3 times, peel off the outer protective layer with a scalpel, then soak in 0.1% mercuric chloride for 2 minutes, and finally rinse with sterile water 3 times, set aside;
[0037] (2) Preparation of culture medium:
[0038] a. Basic medium: WPM medium + 30g / L sucrose + 4.5g / L aga...
Embodiment 2
[0049] A kind of Epimedium Korean tissue culture rapid propagation method, comprises the steps:
[0050](1) Selection and disinfection of explants: In the late April of spring, wild rhizomes of Epimedium korean were taken, with complete overwintering buds, and the overwintering buds were full, and the tiller buds at the root were used as explants, and first rinsed under running water for 3 hours. Clean the surface appendages with washing powder, wash them twice with sterile water on an ultra-clean workbench, disinfect the surface with 75% ethanol for 30 seconds, and then rinse them with sterile water for 5 times; then disinfect with 0.1% mercury chloride for 2 minutes, and use sterile Rinse with water 3 times, peel off the outer protective layer with a scalpel, then soak in 0.1% mercuric chloride for 2 minutes, and finally rinse with sterile water 3 times, set aside;
[0051] (2) Preparation of culture medium:
[0052] a. Basic medium: WPM medium + 30g / L sucrose + 4.5g / L agar...
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