In-vitro tissue culture and propagation method of radix pueraiae plants
A technology of in vitro culture and pueraria, applied in the field of in vitro culture and reproduction of plant tissue, can solve problems such as single mode, and achieve the effect of rich nutrition
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0021] Select potted excellent and robust kudzu vines and cultivate them in a greenhouse. When the vines grow to more than 1m, take materials. Take normal and mature kudzu vines, cut off the leaves and petioles, and cut them into 3-5cm long stems. The collected stems Rinse it with tap water and dry it, disinfect the surface with ethanol with a volume fraction of 70% in the ultra-clean workbench for 30 seconds, rinse with sterile water 2-3 times, then soak with 0.1% mercuric chloride for 8 minutes, and rinse with sterile water Rinse 4-5 times, dry the surface moisture with sterile filter paper, and obtain sterile stem sections; then cut the sterile stem sections into thin slices about 1 mm thick with a sterilized scalpel.
[0022] Thin slices were cut and then inoculated on the callus induction medium with the formula: MS+2,4-D 0.9mg / L+KT 0.3mg / L+sucrose 30g / L+6g / L agar, pH 5.9 , Culture temperature 20-22 ℃, culture under dark conditions.
[0023] After 4-5 days of culture, th...
Embodiment 2
[0027] Select potted excellent and robust kudzu vines and cultivate them in a greenhouse. When the vines grow to more than 1m, take materials. Take the vigorously growing semi-lignified kudzu vines, cut off the leaves and petioles, and cut them into 2-3cm long stems. Rinse the stem section with tap water and dry it, use 70% ethanol surface disinfection treatment with volume fraction in ultra-clean workbench for 20 seconds, rinse 1-2 times with sterile water, then soak for 5 minutes with 0.1% mercuric chloride, Rinse with sterile water for 3-4 times, blot the surface moisture with sterile filter paper, and obtain sterile stem segments; then cut the sterile stem segments into thin slices about 2 mm thick with a sterilized scalpel.
[0028] Cut the thin slices and inoculate them on callus induction medium with formula: MS+2,4-D 0.6mg / L+KT 0.1mg / L+sucrose 30g / L+6g / L agar, pH value 5.9 , Culture temperature 20-22 ℃, culture under dark conditions.
[0029] After 3-5 days of culture...
Embodiment 3
[0034] Select the vigorously growing Pueraria mirifica in the field, cut off the semi-lignified Pueraria vines from the vines of the year, cut off the leaves and petioles, cut into 2-3cm long stems, rinse them with tap water and thoroughly soak them in a solution added with detergent , then rinse it with tap water and dry it. In the ultra-clean workbench, use 70% ethanol to disinfect the surface for 30 seconds, rinse it with sterile water for 1-2 times, and then soak it in 0.1% mercury chloride for 6 minutes. , rinsed with sterile water for 3-4 times, and blotted the surface moisture with sterile filter paper to obtain sterile stem segments; then cut the sterile stem segments into thin slices about 3 mm thick with a sterilized scalpel.
[0035] Thin slices were cut and then inoculated on the callus induction medium with the formula: MS+2,4-D 0.8mg / L+KT 0.2mg / L+sucrose 30g / L+6g / L agar, pH value 5.9 , Culture temperature 20-22 ℃, culture under dark conditions.
[0036] After 3-...
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