Plant tissue culture method by adding culture medium under bacterial environment condition
A technology for plant tissue culture and environmental conditions, applied in botany equipment and methods, plant regeneration, horticultural methods, etc., can solve the problems of limited popularization and application, high investment and technical requirements, high production costs, etc., to reduce costs and simplify cultivation Process and difficulty, effect of promoting plant growth
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Embodiment 1
[0031] The incubator such as Figure 1~3 As shown, it includes a detachable box body (1) and a cover body (2); a seedling tray (5) is placed in the box body (1), and the plastic box main body (1) is 25-35 centimeters long and wide. 18-23 centimeters, 13-15 centimeters high, 0.2-0.3 centimeters from the bottom of the box is provided with an air inlet (4) with a diameter of 0.3-0.5 centimeters; the plastic box cover is 25-35 centimeters long and 18-23 centimeters wide , 1.5-3.0 cm high, with a 0.8-1.0 diameter ventilation hole (3) on the left and right sides, and the cover and the main body are buckled and sealed;
[0032] The length and width of the seedling-carrying tray (5) are smaller than the main body of the plastic box, and the tray has 8-12 holes (6), the diameter of the hole (6) is 5-6 cm, and the diameter of the hole (6) is 2-6 cm. 3 cm, 5-6 cm deep;
Embodiment 2
[0034] (1) prepare the incubator for plant tissue culture;
[0035] (2) After the cultivation incubator is sterilized, put the seedling-carrying tray in the cultivation box, and place it under sterile conditions for standby;
[0036] (3) sugarcane proliferation seedling cluster buds are divided into small cluster seedlings of 2-3 strains, the small cluster seedlings are put into the hole of the seedling-carrying hole of the box main body, add MS medium, cover the cover body, and Continuously inject sterile air into the air inlet for cultivation;
[0037] (4) Add proliferation medium after culturing for 15 days;
[0038] (5) After the hole is full of tissue culture seedlings, add rooting medium to carry out rooting cultivation;
[0039] (6) After the tissue-cultured seedlings take root, remove the culture box for pseudo-planting, and stop feeding sterile air into the culture box.
[0040] The method of adding the proliferation medium described in step (4) and the rooting med...
Embodiment 3
[0054] (1) prepare the incubator for plant tissue culture;
[0055] (2) After the cultivation incubator is sterilized, put the seedling-carrying tray in the cultivation box, and place it under sterile conditions for standby;
[0056] (3) sugarcane proliferation seedling cluster buds are divided into small cluster seedlings of 2-3 strains, the small cluster seedlings are put into the hole of the seedling-carrying hole of the box main body, add MS medium, cover the cover body, and Continuously inject sterile air into the air inlet for cultivation;
[0057] (4) adding proliferation medium after culturing for 20 days;
[0058] (5) After the hole is full of tissue culture seedlings, add rooting medium to carry out rooting cultivation;
[0059] (6) After the tissue-cultured seedlings take root, remove the culture box for pseudo-planting, and stop feeding sterile air into the culture box.
[0060] The method of adding the proliferation medium described in step (4) and the rooting ...
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