A kind of tissue culture propagation method of blood potato
The technology of an inoculation device and a connecting rod is applied in the fields of horticultural methods, botanical equipment and methods, horticulture, etc., which can solve the problems of reducing the reproduction coefficient of blood loose potato, cross-infection, low seed yield, etc., and improve the quality and reproduction of seedlings. coefficient, the effect of promoting differentiation and growth, and increasing the inoculation rate
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Embodiment 1
[0041] The blood scattered potato tissue culture propagation method of the present invention comprises the following steps:
[0042] (1) Acquisition of sterile explants: take bloody potato terminal buds as explants, place them in a beaker, soak them in 0.05% detergent solution by mass for 4 minutes, and gently clean the explants with a brush during the soaking process Surface dirt, then rinsed with running water for 10 minutes; transferred to the ultra-clean workbench, sterilized with 0.1% mercury liter added with 2 drops of Tween-20 for 8 minutes, then rinsed with sterile water for 3 times, and then rinsed with sterile water. Bacteria absorbent paper blots the surface moisture, cuts into 0.5cm stem segments with a terminal bud, and obtains aseptic explants; the sterile water is distilled water after autoclaving;
[0043] (2) Acquisition of sterile test-tube plantlets: inoculate the sterile explants obtained in step (1) into the induction medium, and cultivate under the condit...
Embodiment 2
[0048] The blood scattered potato tissue culture propagation method of the present invention comprises the following steps:
[0049] (1) Acquisition of sterile explants: take bloody potato terminal buds as explants, place them in a beaker, soak them in an aqueous solution of 0.05% detergent solution for 6 minutes, and gently clean the explants with a brush during the soaking process Surface dirt, then rinsed with running water for 20 minutes; transferred to the ultra-clean workbench, sterilized with 0.1% mercury liter added with 3 drops of Tween-20 for 10 minutes, then rinsed with sterile water for 5 times, and then rinsed with sterile water. Bacteria absorbent paper blots the surface moisture, cuts into 0.8cm stem segments with a terminal bud, and obtains aseptic explants; the sterile water is distilled water after autoclaving;
[0050] (2) Acquisition of sterile test-tube plantlets: inoculate the sterile explants obtained in step (1) into the induction medium, and cultivate ...
Embodiment 3
[0055] The blood scattered potato tissue culture propagation method of the present invention comprises the following steps:
[0056] (1) Acquisition of sterile explants: take bloody potato terminal buds as explants, place them in a beaker, soak them in an aqueous solution of 0.05% detergent solution for 5 minutes, and gently clean the explants with a brush during the soaking process Surface dirt, and then rinsed with running water for 15 minutes; transferred to the ultra-clean workbench, sterilized with 0.1% mercury liter added with 2.5 drops of Tween-20 for 9 minutes, then rinsed with sterile water for 4 times, and then rinsed with sterile water. Bacteria absorbent paper blots the surface moisture, cuts into a 0.6cm stem segment with a terminal bud, and obtains aseptic explants; the sterile water is distilled water after autoclaving;
[0057] (2) Acquisition of sterile test-tube plantlets: inoculate the sterile explants obtained in step (1) into the induction medium, and cult...
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Abstract
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