Tissue culture and rapid propagation method for dracaena cochinchinensis
A technology of dragon blood tree and tissue culture, applied in the field of plant reproduction, can solve problems such as difficulty in realizing large-scale cultivation, limited number of seedlings, long time required, etc. The effect of mass production
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Embodiment 1
[0023] An example of the tissue culture rapid propagation method of Dracaena glabrata of the present invention, comprises the following steps:
[0024] (1) Selection and disinfection of explants: Take the seeds of Dracaena glabrata as explants, soak them in 2% detergent solution for 5 minutes, wash them with linear tap water for 15-30 minutes, add 2-3 drops of Tween 100 milliliters of 0.1% mercury liter at -20 were sterilized for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally removed surface moisture with sterile filter paper to obtain explants, wherein the sterile water was distilled water sterilized by high pressure;
[0025] (2) Seed germination to obtain sterile test-tube plantlets: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500lux, and light time of 12-14 hours / day Cultivate under the condition of 30 days, obtain sterile test-tube plantlet after seed germination, wherein in MS med...
Embodiment 2
[0031] Another example of the tissue culture rapid propagation method of Dracaena glabrata of the present invention, comprises the following steps:
[0032](1) Selection and disinfection of explants: Take the seeds of Dracaena glabrata as explants, soak them in 2% detergent solution for 5 minutes, wash them with linear tap water for 15-30 minutes, add 2-3 drops of Tween 100 milliliters of 0.1% mercury liter at -20 were sterilized for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally removed surface moisture with sterile filter paper to obtain explants, wherein the sterile water was distilled water sterilized by high pressure;
[0033] (2) Seed germination to obtain sterile test-tube plantlets: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500lux, and light time of 12-14 hours / day Cultivate under the condition of 30 days, obtain sterile test-tube plantlet after seed germination, wherein in MS...
Embodiment 3
[0039] Another example of the tissue culture rapid propagation method of Dracaena glabrata of the present invention comprises the following steps:
[0040] (1) Selection and disinfection of explants: Take the seeds of Dracaena glabrata as explants, soak them in 2% detergent solution for 5 minutes, wash them with linear tap water for 15-30 minutes, add 2-3 drops of Tween 100 milliliters of 0.1% mercury liter at -20 were sterilized for 8-10 minutes, rinsed with sterile water for 3-5 times, and finally removed surface moisture with sterile filter paper to obtain explants, wherein the sterile water was distilled water sterilized by high pressure;
[0041] (2) Seed germination to obtain sterile test-tube plantlets: Inoculate the explants obtained in step (1) into MS medium at a culture temperature of 23-27°C, light intensity of 1500lux, and light time of 12-14 hours / day Cultivate under the condition of 30 days, obtain sterile test-tube plantlet after seed germination, wherein in MS...
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