Method for in-vitro culture of stem apexes of sweet potatoes and virus detection of tissue culture seedlings
A virus detection and in vitro culture technology, applied in horticultural methods, botanical equipment and methods, biochemical equipment and methods, etc., to achieve the effects of high virus detection accuracy, improved success rate, and effective detection methods
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Embodiment 1
[0017] A method for in vitro culture of sweet potato shoot tips and virus detection in tissue cultured seedlings, the specific steps are:
[0018] (1) Material collection and disinfection
[0019] Cut off the top buds of sweet potato seedlings growing vigorously in the field in June, cut off the leaves, rinse with tap water for 40 minutes, blot the water with sterile filter paper, put it on a clean workbench and soak it with 75% alcohol for 25 seconds, and then use 0.1% L Mercury disinfection for 5 minutes, finally rinsed with sterile water for 7 times, and set aside;
[0020] (2) Shoot tip stripping and cultivation
[0021] Under the binocular dissecting microscope, peel off the outer leaves of the sterilized sweet potato terminal buds with the tip of a syringe, leaving only one leaf primordium, and inoculate five shoot tips with a size of 0.1mm on the primary medium for cultivation. The medium sucrose is 30g / L, the agar is 6.0g / L, the pH is 5.8, the culture temperature is ...
Embodiment 2
[0027] A method for in vitro culture of sweet potato shoot tips and virus detection in tissue cultured seedlings, the specific steps are:
[0028] (1) Material collection and disinfection
[0029] Cut off the top buds of sweet potato seedlings growing vigorously in the field in June, cut off the leaves, rinse with tap water for 50 minutes, blot the water with sterile filter paper, place it on a clean bench and soak it with 75% alcohol for 25 seconds, and then rinse it with 0.1% L Mercury disinfection for 5 minutes, finally rinsed with sterile water 8 times, and set aside;
[0030] (2) Shoot tip stripping and cultivation
[0031] Under the binocular dissecting microscope, peel off the outer leaves of the sterilized sweet potato terminal buds with the tip of a syringe, leaving only 2 leaf primordia, and inoculate 6 shoot tips with a size of 0.2mm on the primary medium for cultivation. The medium sucrose is 30g / L, the agar is 6.0g / L, the pH is 5.8, the culture temperature is 25...
Embodiment 3
[0037] A method for in vitro culture of sweet potato shoot tips and virus detection in tissue cultured seedlings, the specific steps are:
[0038] (1) Material collection and disinfection
[0039] Cut off the top buds of sweet potato seedlings growing vigorously in the field in June, cut off the leaves, rinse with tap water for 45 minutes, blot the water with sterile filter paper, place it on a clean bench and soak it with 75% alcohol for 25 seconds, and then rinse it with 0.1% L Mercury disinfection for 5 minutes, finally rinsed with sterile water 8 times, and set aside;
[0040] (2) Shoot tip stripping and cultivation
[0041] Under the binocular dissecting microscope, peel off the outer leaves of the sterilized sweet potato terminal buds with the tip of a syringe, leaving only one leaf primordium, and inoculate 6 shoot tips with a size of 0.2mm on the primary medium for cultivation. The medium sucrose is 30g / L, the agar is 6.0g / L, the pH is 5.8, the culture temperature is...
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