Rapid propagation method for culturing suspension cells of swertia pseudochinensis
A technology of swede swede and suspended cells, which is applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve problems such as the lack of research on cultivation methods, and achieves advantages of large-scale planting, short cycle and low pollution. Effect
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Embodiment 1
[0009] Take the Swertia pilosa seeds, wash them, soak them in washing powder for 25 minutes, rinse them with running water for 2.5 hours, treat them with 75% alcohol on an ultra-clean workbench for 10 minutes, treat them with 0.2% mercury chloride for 23 minutes, rinse them with sterile water 5 times, and disinfect them The treated seeds were placed and inserted into the H+NAA0.01mg / L+6-BA0.3mg / L+ZT0.8mg / L medium in the light incubator for callus induction, with 7g / L agar added, 30g / L L sucrose, temperature 25°C, the induced callus was inserted into medium H+ZT0.5mg / L+KT0.5mg / L for callus proliferation culture, additional 7g / L agar, 30g / L sucrose, light 3500lx, light time 12h / d, temperature 25°C, callus with emerald green color and uniform structure after proliferation, inoculate into H+ZT0.3mg / L+KT0.3mg / L medium for suspension shaking culture, add 30g / L sucrose, temperature 25°C, light 3500lx, light time 12h / d, amplitude 3cm, vibration frequency 100r / min, suspension cell gro...
Embodiment 2
[0011] Take the Swertia pilosa seeds, wash them, soak them in washing powder for 25 minutes, rinse them with running water for 2.5 hours, treat them with 75% alcohol on an ultra-clean workbench for 10 minutes, treat them with 0.2% mercury chloride for 23 minutes, rinse them with sterile water 5 times, and disinfect them The treated seeds were placed and inserted into the H+NAA0.01mg / L+6-BA0.3mg / L+ZT0.8mg / L medium in the light incubator for callus induction, with 7g / L agar added, 30g / L L sucrose, temperature 25°C, the induced callus was inserted into medium H+ZT0.5mg / L+KT0.5mg / L for callus proliferation culture, additional 7g / L agar, 30g / L sucrose, light 3500lx, light time 12h / d, temperature 25°C, callus with emerald green color and uniform structure after proliferation, inoculated into H+ZT0.5mg / L+KT0.5mg / L medium for suspension shaking culture, add 30g / L sucrose, temperature 25°C, light 3500lx, light time 12h / d, amplitude 3cm, vibration frequency 100r / min, growth rate of sus...
Embodiment 3
[0013] Take the Swertia pilosa seeds, wash them, soak them in washing powder for 25 minutes, rinse them with running water for 2.5 hours, treat them with 75% alcohol on an ultra-clean workbench for 10 minutes, treat them with 0.2% mercury chloride for 23 minutes, rinse them with sterile water 5 times, and disinfect them The treated seeds were placed and inserted into the H+NAA0.01mg / L+6-BA0.3mg / L+ZT0.8mg / L medium in the light incubator for callus induction, with 7g / L agar added, 30g / L L sucrose, temperature 25°C, the induced callus was inserted into medium H+ZT0.5mg / L+KT0.5mg / L for callus proliferation culture, additional 7g / L agar, 30g / L sucrose, light 3500lx, light time 12h / d, temperature 25°C, callus with emerald green color and uniform structure after proliferation, inoculate into H+ZT0.3mg / L+KT0.5mg / L medium for suspension shaking culture, add 30g / L sucrose, temperature 25°C, light 3500lx, light time 12h / d, amplitude 3cm, vibration frequency 100r / min, suspension cell gro...
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