Chinese scholartree detached leaf somatic embryo induction rapid-breeding method
A technology of isolated leaves and somatic embryos, applied in the field of plant biology, can solve the problems of less budding and low regeneration rate of Sophora japonica, and achieve the effect of saving time.
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Embodiment 1
[0048] Select a single plant with strong growth and excellent performance, take its young shoots that are free from diseases and insect pests, remove excess stems and leaves, wash carefully with detergent, and rinse with running water for 1 hour. After cleaning, cut into appropriate sizes and prepare for disinfection .
[0049] Put the test material on the ultra-clean workbench, disinfect with 70% alcohol for 30 seconds, rinse with sterile water for 3 times, then sterilize with 0.1% mercuric chloride for 10 minutes, rinse with sterile water for 5 times, and dry the water with sterile filter paper , and then cut about 1 cm of the stem segment with an axillary bud or terminal bud, and insert it vertically into the bud initiation medium (MS+5.0g / L agar+30g / L sucrose, pH 5.8). Three stem segments were inoculated in each bottle to induce the germination of terminal buds and axillary buds. After 15 days of cultivation, the axillary buds or terminal buds of the stems begin to germin...
Embodiment 2
[0061] Select a single plant with strong growth and excellent performance, take its young shoots that are free from diseases and insect pests, remove excess stems and leaves, wash carefully with detergent, and rinse with running water for 1 hour. After cleaning, cut into appropriate sizes and prepare for disinfection .
[0062] Put the test material on the ultra-clean workbench, disinfect with 70% alcohol for 40 seconds, rinse with sterile water for 4 times, then sterilize with 0.1% mercuric chloride for 12 minutes, rinse with sterile water for 6 times, and dry the water with sterile filter paper , and then cut about 1 cm of the stem segment with an axillary bud or terminal bud, and insert it vertically into the bud initiation medium (MS+5.0g / L agar+30g / L sucrose, pH 5.8). Inoculate 3 stem segments per bottle to induce bud germination. After 18 days of cultivation, the axillary buds or terminal buds of the stems began to germinate, and the stem tips elongated obviously, and t...
Embodiment 3
[0073] Select a single plant with strong growth and excellent performance, take its young shoots that are free from diseases and insect pests, remove excess stems and leaves, wash carefully with detergent, and rinse with running water for 1 hour. After cleaning, cut into appropriate sizes and prepare for disinfection .
[0074] Put the test material on the ultra-clean workbench, disinfect with 70% alcohol for 60 seconds, rinse with sterile water for 3 times, then sterilize with 0.1% mercuric chloride for 15 minutes, rinse with sterile water for 6 times, and dry the water with sterile filter paper , and then cut about 1 cm of the stem segment with an axillary bud or terminal bud, and insert it vertically into the bud initiation medium (MS+5.0g / L agar+30g / L sucrose, pH 5.8). Inoculate 3 stem segments per bottle to induce bud germination. After 20 days of cultivation, the axillary buds or terminal buds of the stems begin to germinate, and the stem tips elongate obviously, and th...
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