Chrysanthemum simplified tissue culturing method
A tissue culture, chrysanthemum technology, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of restricting general promotion to the market, long lighting cultivation, increasing costs, etc., to achieve good theoretical research value, good production and application. Prospects, the effect of reducing production costs
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Embodiment 1
[0019] For tissue culture in this example, a special tissue culture room is required, the temperature is controlled by an air conditioner to (25±1)°C, and the light intensity is 3000-4000 lx by using an incandescent lamp every day for 8 hours and 16 hours in the dark. The culture medium and various utensils required for inoculation were put into a pressure cooker for sterilization, and after natural cooling, they were taken out and put into the inoculation room for use. Take MS as the basic medium, sucrose 30g / L, agar 6g / L, pH value adjusted to 5.8, additional 6-BA0.3mg / L+NAA0.3mg / L+IBA0.1mg / L, medium at 121 ℃ Sterilize at high temperature for 16 minutes for use; select robust shoots of the current year, and use the lateral buds in the middle of the full but ungerminated shoots as explants. Remove the leaves from the branches, cut them into 2-3cm pieces with side buds, wash them with clean water, and then dry them with filter paper. First, disinfect with 75% alcohol for 20s u...
Embodiment 2
[0021] For tissue culture in this example, a special tissue culture room is required, the temperature is controlled by an air conditioner to (25±1)°C, and the light intensity is 3000-4000 lx by using an incandescent lamp every day for 8 hours and 16 hours in the dark. The culture medium and various utensils required for inoculation were put into a pressure cooker for sterilization, and after natural cooling, they were taken out and put into the inoculation room for use. Take MS as the basic medium, sucrose 30g / L, agar 6g / L, pH value adjusted to 5.8, additional 6-BA0.3mg / L+NAA0.3mg / L+IBA0.1mg / L, medium at 121 ℃ Sterilize at high temperature for 16 minutes for use; select robust shoots of the current year, and use the lateral buds in the middle of the full but ungerminated shoots as explants. Remove the leaves from the branches, cut them into 2-3cm pieces with side buds, wash them with clean water, and then dry them with filter paper. First, disinfect with 75% alcohol for 20s u...
Embodiment 3
[0023] For tissue culture in this example, a special tissue culture room is required, the temperature is controlled by an air conditioner to (25±1)°C, and an incandescent lamp is used to illuminate for 8 hours a day, dark for 16 hours, and the light intensity is 3000-4000 lx. The culture medium and various utensils required for inoculation were put into a pressure cooker for sterilization, and after natural cooling, they were taken out and put into the inoculation room for use. Take MS as the basic medium, sucrose 30g / L, agar 6g / L, pH value adjusted to 5.8, additional 6-BA0.3mg / L+NAA0.3mg / L+IBA0.1mg / L, medium at 121 ℃ Sterilize at high temperature for 16 minutes for use; select robust shoots of the current year, and use the lateral buds in the middle of the full but ungerminated shoots as explants. Remove the leaves from the branches, cut them into 2-3cm pieces with side buds, wash them with clean water, and then dry them with filter paper. First, disinfect with 75% alcohol f...
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