Method for establishing tissue culture rapid propagation system of single-leaf robinia. pseudoacacia
A technology of tissue culture and rapid propagation of black locust single leaf, which is applied in the field of plant tissue culture, and can solve the problems of not being able to meet the needs of black locust seedlings, low reproduction coefficient, and long cycle
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0016] (1) Start-up culture: Select the annual lignified stem section with buds of robust Robinia unileaf plant as explants, cut off the leaves, cut into 3.0-5.0 long segments with 2-3 axillary buds, and wash them with washing powder water first. Rinse for 1 hour, then gently scrub the surface of the explants with a soft brush to remove the dust and some bacteria on the surface, then rinse with tap water for 1 hour, then place it in an ultra-clean workbench, first sterilize it with 75% ethanol for 5 seconds, and then use a sterile Wash 3 times with water, then sterilize with 0.1% mercuric chloride solution for 10 minutes, rinse 4 times with sterile water, dry the water droplets on the surface with sterile filter paper, inoculate into the starting medium for induction culture, and inoculate at 28°C after inoculation. Cultivate in total darkness for 2 days, then place in the light for 10 hours per day, and cultivate for 5 days under the condition of light intensity of 1500lx to s...
Embodiment 2
[0021] (1) Start-up culture: Select the annual lignified stem section with buds of robust Robinia unileaf plant as explants, cut off the leaves, cut into 3.0-5.0 long segments with 2-3 axillary buds, and wash them with washing powder water first. Rinse for 1 hour, then gently brush the surface of the explants with a soft brush to remove the dust and some bacteria on the surface, then rinse with tap water for 2 hours, then place it in an ultra-clean workbench, first sterilize it with 75% ethanol for 8 seconds, and then use a sterile Wash 3 times with water, then sterilize with 0.1% mercuric chloride solution for 15 minutes, rinse 4 times with sterile water, dry the water droplets on the surface with sterile filter paper, inoculate into the starting medium for induction culture, and inoculate at 28°C after inoculation. Cultivate in total darkness for 2 days, and then place it in the light for 11 hours a day, and cultivate for 7 days under the condition of light intensity of 1500l...
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