In-vitro rapid propagation method for tissue culture of broad-leafed notopterygium
A technology of notopterygia broadleaf and tissue culture, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of tissue culture that have not been reported yet, and achieve good biological characteristics, good synchronization, and fast emergence Effect
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Embodiment 1
[0027] Example 1 A method for in vitro rapid propagation of Notopterygia broadleaf tissue culture, comprising the following steps:
[0028] (1) Selection and disinfection of explants: use the root buds of Notopterygium broadleaf as explants, wash them with running water for 15 minutes, soak them in alcohol with a volume concentration of 75% for 20 seconds, and then rinse them with sterile deionized water 2 to 3 times, then put the washed explants in mercuric chloride with a mass concentration of 0.1%, soak and sterilize for 8 minutes, rinse with sterile deionized water for 3 times, and finally dry the water with sterile filter paper. Single buds of explants after disinfection were obtained.
[0029] (2) Inoculation of explants: Inoculate single buds of sterilized explants on the induction bud differentiation medium, wherein one sterilized single bud of explants is inoculated in every 25ml of induction bud differentiation medium; at a temperature of 20°C ±2℃, the light s...
Embodiment 2
[0038] Example 2 A method for in vitro rapid propagation of Notopterygia broadleaf tissue culture, comprising the following steps:
[0039] (1) Selection and disinfection of explants: use the root buds of Notopterygium broadleaf as explants, wash them with running water for 20 minutes, soak them in alcohol with a volume concentration of 75% for 25 seconds, and then rinse them with sterile deionized water 2 to 3 times, then put the washed explants in mercuric chloride with a mass concentration of 0.15%, soak and sterilize for 10 minutes, and rinse with sterile deionized water for 3 times, and finally dry the water with sterile filter paper. Single buds of explants after disinfection were obtained.
[0040] (2) Inoculation of explants: Inoculate single buds of sterilized explants on the induction bud differentiation medium, wherein one sterilized single bud of explants is inoculated in every 25ml of induction bud differentiation medium; at a temperature of 20°C ±2℃, the l...
Embodiment 3
[0049] Example 3 A method for in vitro rapid propagation of Notopterygia broadleaf tissue culture, comprising the following steps:
[0050](1) Selection and disinfection of explants: use the root buds of Notopterygium broadleaf as explants, wash them with running water for 25 minutes, soak them in alcohol with a volume concentration of 75% for 30 seconds, and then rinse them with sterile deionized water 2 to 3 times, then put the washed explants in mercuric chloride with a mass concentration of 0.2%, soak and sterilize for 12 minutes, and rinse 4 times with sterile deionized water, and finally dry the water with sterile filter paper. Single buds of explants after disinfection were obtained.
[0051] (2) Inoculation of explants: Inoculate single buds of sterilized explants on the induction bud differentiation medium, wherein one sterilized single bud of explants is inoculated in every 25ml of induction bud differentiation medium; at a temperature of 20°C ±2℃, the light s...
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