Quick virus-free group-cultivating and propagating method of OT type lily of hybrid group
A hybrid and tissue culture technology, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of bulb buds prone to genetic variation, prone to vitrification, incomplete detoxification, etc. Effects of necrosis, overcoming decreased viability, refrigeration and prolonged colonization period
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0033] Embodiment 1: (OT type hybrid line lily virus-free tissue culture rapid propagation method 1)
[0034] The specific method is as follows:
[0035] (1) Preparation and standby of the culture medium: the components including the basic medium and the culture medium at each stage of tissue culture and the weight of each component in each liter of culture medium are formulated as follows.
[0036] (2) Selection and sterilization of explants: In early March, the dormant and broken bulbs were taken, treated with heat and humidity at 50°C for 70 minutes, soaked in 75% alcohol for 0.5 minutes, rinsed with sterile water for 3 to 5 times, and then Sterilize with 0.1% mercuric chloride solution for 15 minutes, rinse with sterile water for 3 to 5 times, sterilize with 10% sodium hypochlorite aqueous solution for 15 minutes, and finally rinse with sterile water for 3 to 5 times, as explants for detoxification tissue culture .
[0037] (3) Induction culture: Take a 0.2-0.3mm shoot t...
Embodiment 2
[0043] Embodiment 2: (OT type hybrid line lily virus-free tissue culture rapid propagation method 2)
[0044] (1) Preparation and standby of the culture medium: the components including the basic medium and the culture medium at each stage of tissue culture and the weight of each component in each liter of culture medium are formulated as follows.
[0045] (2) Selection and sterilization of explants: In mid-March, take bulbs that have been broken from dormancy, heat and treat them at 50°C for 90 minutes, soak them in 75% alcohol for 1.0 minutes, wash them with sterile water for 3 to 5 times, and then Sterilize with 0.1% mercuric chloride solution for 20 minutes, rinse with sterile water for 3 to 5 times, sterilize with 10% sodium hypochlorite aqueous solution for 13 minutes, and finally rinse with sterile water for 3 to 5 times, as explants for detoxification tissue culture .
[0046] (3) Induction culture: Take a 0.2-0.3mm shoot tip under the objective lens and inoculate it ...
Embodiment 3
[0052] Embodiment 3: (OT type hybrid line lily virus-free tissue culture rapid propagation method 3)
[0053] (1) Preparation and standby of the culture medium: the components including the basic medium and the culture medium at each stage of tissue culture and the weight of each component in each liter of culture medium are formulated as follows.
[0054] (2) Selection and sterilization of explants: In the first ten days of March, the dormant and broken bulbs were taken, treated with heat and humidity at 50°C for 80 minutes, soaked in 75% alcohol for 0.75 minutes, rinsed with sterile water 3 to 5 times, and then Sterilize with 0.1% mercuric chloride solution for 18 minutes, rinse with sterile water for 3 to 5 times, sterilize with 10% sodium hypochlorite aqueous solution for 14 minutes, and finally rinse with sterile water for 3 to 5 times, as explants for detoxification tissue culture .
[0055] (3) Induction culture: Take a 0.2-0.3mm shoot tip under the objective lens 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