A complete medium for inducing rapid propagation of somatic embryos from isolated leaves of Sophora japonica
A technology of isolated leaves and culture medium, applied in application, horticulture, botanical equipment and methods, etc., can solve the problems of less budding, long induction time of immature zygotic embryos, and low regeneration rate, and achieve the effect of saving time.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0036] Select a single plant with strong growth and excellent performance, and 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 .
[0037]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 ger...
Embodiment 2
[0049] Select a single plant with strong growth and excellent performance, and 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 .
[0050] 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 begin to germinate, and the stem tips elongate obviously, an...
Embodiment 3
[0062] Select a single plant with strong growth and excellent performance, and 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 .
[0063] 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% mercury 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...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com