Method for in vitro and rapid propagation of Dieffenbachia tiger-eye with flower stalk as explant
A technology of explants and explants, which can be used in botany equipment and methods, horticultural methods, plant regeneration, etc., can solve unfavorable subculture, low reproduction coefficient, and limit the application of tissue culture technology of tiger eye. problems, to achieve the effect of low cost, efficient regeneration system, and low variation of regenerated plants
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Embodiment 1
[0012] 1. Inoculation of explants and induction of callus: cut off the young flower stalk at the lower end of the tiger's eye flower, put the young flower stalk into a sterile ultra-clean bench, and use 75% (volume / volume) alcohol Soak for 1 minute, soak in 0.2% (mass / volume) mercuric solution for 5 minutes, and rinse with sterile water 5 times. The young flower stalks were cut into small pieces with a length of 3 to 5 mm, and inoculated on MS medium containing 6-BA 2 mg / L, IBA 0.15 mg / L, sucrose 3.5% (mass / volume), and pH 6.2. 20 ℃ ~ 30 ℃ 4 ~ 6 hours of fluorescent light every day, light intensity 1500 ~ 2000Lux. Subculture once every 25 days, and differentiation can be induced when yellow-green callus grows.
[0013] 2. Induction of adventitious buds: transfer the yellow-green callus to MS containing NAA (0.15mg / L)+KT (2.0mg / L)+agar (7g / L)+4.0% sucrose (mass / volume) Induction differentiation medium, pH 6.1, subculture once every 40 days, 20 ℃ ~ 30 ℃ daily fluorescent light...
Embodiment 2
[0017] 1. Inoculation of explants and induction of callus: cut off the young flower stalk at the lower end of the tiger's eye flower, put the young flower stalk into a sterile ultra-clean bench, and use 75% (volume / volume) alcohol Soak for 2 minutes, soak with 0.1% (mass / volume) mercuric chloride solution for 10 minutes, and rinse with sterile water for 5 times. The young flower stalks were cut into small pieces with a length of 3-5 mm, and inoculated in MS medium containing 6-BA 2.2 mg / L, IBA 0.1 mg / L, sucrose 3.8% (mass / volume), and pH 5.8 On, 20 ℃ ~ 30 ℃ 4 ~ 6 hours of fluorescent light every day, light intensity 1500 ~ 2000Lux. Subculture once every 28 days, and differentiation can be induced even when yellow-green callus grows.
[0018] 2. Induction of adventitious buds: transfer the yellow-green callus to MS containing NAA (0.4 mg / L) + KT (2.0 mg / L) + agar (5 g / L) + 3.5% sucrose (mass / volume). Induction differentiation medium, pH 5.5, subculture once every 45 days, 20 ...
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