Rapid propagation method for xanthoceras sorbifolia bunge tissue during culturing
A technology of tissue culture and sorbifolium, applied in the field of plant tissue culture, can solve the problems of difficult rooting, low callus induction rate, browning, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0019] 1. Treatment of explants: Select the mature embryos of X. sorbifolium as explants, place them in warm water at 60°C and cool them down to room temperature for 5 hours, and then disinfect them with 0.1% mercuric chloride solution containing 0.01% Tween-20 2min, washed 5 times with sterile water, peeled off the seed coat, soaked in 75% ethanol solution for 20s, rinsed 5 times with sterile water, and then sterilized with 0.1% mercuric chloride solution containing 0.01% Tween-20 for 2 minutes. Bacterial water was washed 5 times before inoculation, and the success rate was 65%.
[0020] 2. Callus induction: cut the sterilized seed embryo into about 3-5mm 3 The tissue pieces were inoculated on the induction medium for callus induction culture. After inoculation, they were first cultured in total darkness at 25°C for 20 days, and then placed in light for 10 hours a day, with a light intensity of 1500x and a culture temperature of 25°C. Culture under the conditions until callu...
Embodiment 2
[0026] 1. Treatment of explants: Select the mature embryos of X. sorbifolium as explants, place them in warm water at 70°C and cool them down to room temperature for 5 hours, and then sterilize them with 0.1% mercuric chloride solution containing 0.03% Tween-20 5min, washed 3 times with sterile water, peeled off the seed coat, soaked in 78% ethanol solution for 25s, rinsed 5 times with sterile water, and then sterilized with 0.1% mercuric chloride solution containing 0.03% Tween-20 for 5min. Bacterial water was washed 5 times before inoculation, and the success rate was 73%.
[0027] 2. Callus induction: cut the sterilized seed embryo into about 3-5mm 3 The tissue pieces were inoculated on the induction medium for callus induction culture. After inoculation, they were cultured in total darkness at 28°C for 23 days, and then placed in the light for 11 hours a day, with a light intensity of 1500x and a culture temperature of 28°C. Culture under the conditions until callus is fo...
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