A method for hardening and transplanting of callus-induced T.
A technology of callus induction and exposure to martinis, which is applied in horticultural methods, botany equipment and methods, plant regeneration, etc., can solve the problems of low survival rate, reduced survival rate, limited buffer capacity, etc., and reduce transplanting death rate, increase the survival rate, and increase the effect of resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0041] (1) Select the mature seeds of S. japonica, clean them with washing powder, and then rinse them with water for 1 hour; place them on an ultra-clean workbench and soak them in 75% ethanol by volume for 30 seconds, and rinse them with sterile water 3 times, air-dried on sterile filter paper, then sterilized with 0.1% mercury liter for 8 minutes, and then rinsed with sterile water 3 times to obtain sterilized seeds;
[0042] (2) Cut the sterilized seeds, insert the hypocotyls into the MS culture medium and cultivate them. The culture conditions are: the culture temperature is 22° C., the light intensity is 2000 lx, the light time is 12 hours per day, and cultured for 10 days. hypocotyl;
[0043] (3) Get 5mm hypocotyls and inoculate them on the callus induction medium that uses MS solid medium as the basic medium and contains 5mg / LBA and 0.5mg / LIBA, at a temperature of 20°C and a light intensity of 2000lx , 12 hours of light per day, cultured for 50 days, and callus tissue...
Embodiment 2
[0048] (1) Select the mature seeds of S. japonica, clean them with washing powder, and then rinse them with water for 2 hours; place them on the ultra-clean workbench and soak them in 75% ethanol for 30 seconds, and rinse them with sterile water 3 times, air-dried on sterile filter paper, then sterilized with 0.1% mercury liter for 8 minutes, and then rinsed with sterile water 3 times to obtain sterilized seeds;
[0049] (2) Cut the sterilized seeds, insert the hypocotyls into the MS culture medium and cultivate them. The culture conditions are: the culture temperature is 20° C., the light intensity is 2000 lx, the light time is 12 hours per day, and cultured for 10 days. hypocotyl;
[0050] (3) Get 6mm hypocotyls and inoculate them on the callus induction medium that uses MS solid medium as the basic medium and contains 5mg / LBA and 0.5mg / LIBA, at a temperature of 20°C and a light intensity of 2000lx , light 12h every day, culture for 40 days, get callus;
[0051] (4) Inocul...
Embodiment 3
[0055] (1) Select the mature seeds of Pamarinica, clean them with washing powder, and then rinse them with water for 1.5 hours; place them on an ultra-clean workbench and soak them in ethanol with a volume percentage of 75% for 30 seconds, and rinse them with sterile water Rinse 5 times, air-dry on sterile filter paper, then sterilize with 0.1% mercuric chloride for 8 minutes, then rinse 3 times with sterile water to obtain sterilized seeds;
[0056] (2) Cut the sterilized seeds, insert the hypocotyls into the MS culture medium and cultivate them. The culture conditions are: the culture temperature is 24°C, the light intensity is 2000lx, the light time is 12h per day, and cultured for 10 days. hypocotyl;
[0057] (3) Get 7mm hypocotyls and inoculate them on the callus induction medium that uses MS solid medium as the basic medium and contains 5mg / LBA and 0.5mg / LIBA, at a temperature of 20°C and a light intensity of 2000lx , 12 hours of light per day, cultured for 60 days, 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