Breeding method of gerbera hybrida tissue culture plug seedlings
A tissue culture hole and plug seedling technology is applied in the breeding field of plant tissue culture plug seedlings to achieve the effects of improving the uniformity of seedlings and the speed of reproduction.
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Embodiment 1
[0038] (1) Obtaining sterile materials
[0039] Take young gerbera flower buds with a diameter of less than 1cm and no florets exposed, rinse them with running water for 20 minutes, then place the buds in a sterile bottle in an ultra-clean workbench, soak them in 70% alcohol for 30 seconds, add 0.1% mercury liter Its volume is soaked in 0.1% Tween-80 for 8 minutes, and then rinsed with sterile water for 4-6 times before use.
[0040] (2) Induction and differentiation of adventitious buds
[0041] Use tweezers to peel off all the bracts on the buds from the sterile material obtained in step (1), then cut off the florets on the surface of the buds and the base of the bracts, and the remaining receptacle, cut the receptacle into 4 pieces, and inoculate them on adventitious buds to induce differentiation On the culture medium, place the culture bottle at a temperature of 25°C, light intensity of 1500-2500lx, and light time of 14 hours / day for cultivation. The explants will expand...
Embodiment 2
[0056] (1) Obtaining sterile materials
[0057] Take young gerbera flower buds with a diameter of less than 1cm and no florets exposed, rinse them with running water for 20 minutes, then place the buds in a sterile bottle in an ultra-clean workbench, soak them in 70% alcohol for 30 seconds, add 0.1% mercury liter Its volume is soaked in 0.1% Tween-80 for 10 minutes, and then rinsed with sterile water for 6 times before use.
[0058] (2) Induction and differentiation of adventitious buds
[0059] Use tweezers to peel off all the bracts on the buds from the sterile material obtained in step (1), then cut off the florets on the surface of the buds and the base of the bracts, and the remaining receptacle, cut the receptacle into 4 pieces, and inoculate them on adventitious buds to induce differentiation On the culture medium (same as in Example 1), the culture bottle was placed at a temperature of 25°C, with a light intensity of 1500-2500lx and a light time of 14 hours / day. The e...
Embodiment 3
[0071] (1) Obtaining sterile materials
[0072] Take young gerbera flower buds with a diameter of less than 1cm and no florets exposed, rinse them with running water for 20 minutes, then place the buds in a sterile bottle in an ultra-clean workbench, soak them in 70% alcohol for 30 seconds, add 0.1% mercury liter Its volume is soaked in 0.1% Tween-80 for 10 minutes, and then rinsed with sterile water for 4 times before use.
[0073] (2) Induction and differentiation of adventitious buds
[0074] Use tweezers to peel off all the bracts on the buds from the sterile material obtained in step (1), then cut off the florets on the surface of the buds and the base of the bracts, and the remaining receptacle, cut the receptacle into 4 pieces, and inoculate them on adventitious buds to induce differentiation On the culture medium (same as in Example 1), the culture bottle was placed at a temperature of 25°C, with a light intensity of 1500-2500lx and a light time of 14 hours / day. The e...
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