Method for breeding chamomile
The technology of chamomile and seeds is applied in the field of plant tissue culture, and can solve the problems of unfavorable large-scale chamomile, industrialized production and cultivation, low callus induction rate and adventitious bud differentiation rate, and failure to obtain a chamomile regeneration system, To achieve the effect of promoting callus growth, good growth state and consistent size
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0052] 1. Test materials
[0053] 1. Camomile seeds: collected from the campus of Beijing Forestry University in the autumn of 2009. The planting plants grew well, the seeds were mature and full, and the seed coats were intact.
[0054] 2. Plant growth regulator
[0055] The plant growth regulator used in the present invention adopts domestic naphthalene acetic acid (NAA), 6-benzylamino adenine (6-BA) and 2,4-dichlorophenoxyacetic acid (2,4-D).
[0056] 3. Preparation of culture medium:
[0057] (1) The composition or preparation method of "MS basic medium";
[0058] Table 1 MS medium (Murashige and Skoog, 1962)
[0059]
[0060] After the above MS medium stock solution is prepared, it should be stored in a refrigerator at 4°C until use. According to the quantity of the preparation medium, weigh the required agar and sucrose, pour them into sterile water of 3 / 4 of the volume of the medium to be prepared, and sequentially add the required macroelement mother liquor, trace element mother l...
Embodiment 2
[0092] The culture time is 5 days except for sterile seedlings; 2,4-D 0.5mg / L, 6-BA 0.1mg / L used in callus induction medium; NAA 0.2mg / L used in rooting medium; light for adventitious bud differentiation culture Except for the period of 14 hours of light / 10 hours of darkness, the others are the same as in Example 1.
Embodiment 3
[0094] Except for aseptic seedlings, the culture time is 6 days; the callus induction medium uses 2,4-D 1.0mg / L, 6-BA 1.0mg / L; the adventitious bud differentiation culture light cycle is 14 hours of light / 10 hours of darkness; The rooting medium used NAA 0.3 mg / L, and the photoperiod was 14 hours of light / 10 hours of darkness, and everything else was the same as in Example 1.
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