Vitro rapid propagation method of kefir lily by using tender petals as explant
A technology for explants and Clivia, which is applied to the field of asexual and rapid propagation of flowers, can solve problems such as limiting the application of Clivia tissue culture technology, and achieve the effects of efficient and rapid reproduction, low variation, and high-efficiency regeneration system.
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Embodiment 1
[0012] 1. Explant inoculation and callus induction: the development degree of the young inflorescences obtained is: the size of the flower buds has been or is nearly fully developed but is still green. Put it into a sterile ultra-clean bench, soak it with 75% (volume / volume) alcohol for 30 seconds, soak it with 0.1% (mass / volume) mercuric chloride solution for 10 minutes, and rinse it with sterile water three times. Cut the bud from the uppermost part of the ovary, then cut off most of the upper part of the bud, cut the remaining middle part longitudinally twice, and inoculate it in a medium containing 6-BA0.2mg / L, 2,4-D0.1mg / L, 3% sucrose 40W fluorescent lamp was irradiated for 2 hours per day at 20°C on MS medium. Subculture once every 30 days, and induce differentiation when the yellow-green callus grows.
[0013] 2. Induction of adventitious buds: transfer the yellow-green callus to the induction differentiation medium: MS+6-BA0.5mg / L+2, 4-D0.1+3% sucrose, subculture once...
Embodiment 2
[0017] 1. Explant inoculation and callus induction: The development degree of the young inflorescences obtained is: the size of the flower buds has been or is nearly fully developed but is still green. The flower buds of this development degree are cut from the lower end of the ovary and removed. Cut it open, put it into a sterile ultra-clean bench, soak it with 75% (volume / volume) alcohol for 60 seconds, soak it with 0.2% (mass / volume) mercuric chloride solution for 3 minutes, and rinse it with sterile water 5 times. Cut the bud from the uppermost part of the ovary, then cut off most of the upper part of the bud, cut the remaining middle part longitudinally twice, and inoculate it in a medium containing 6-BA0.2mg / L, 2,4-D0.5mg / L, 3.5% sucrose MS culture medium, irradiated with 40W fluorescent lamp for 4 hours per day at 28°C. Subculture once every 50 days, and induce differentiation when the yellow-green callus grows.
[0018] 2. Induction of adventitious buds: transfer the ...
Embodiment 3
[0022] 1. Explant inoculation and callus induction: The development degree of the young inflorescences obtained is: the size of the flower buds has been or is nearly fully developed but is still green. The flower buds of this development degree are cut from the lower end of the ovary and removed. Cut it open, put it into a sterile ultra-clean bench, soak it with 75% (volume / volume) alcohol for 45 seconds, soak it with 0.15% (mass / volume) mercuric chloride solution for 8 minutes, and rinse it with sterile water 4 times. Cut the bud from the uppermost part of the ovary, then cut off most of the upper part of the bud, cut the remaining middle part longitudinally twice, and inoculate it in a medium containing 6-BA0.2mg / L, 2,4-D0.3mg / L, 3.2% sucrose MS culture medium, irradiated with 40W fluorescent lamp for 3 hours per day at 25°C. Subculture once every 45 days, and induce differentiation when the yellow-green callus grows.
[0023] 2. Induction of adventitious buds: transfer the...
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