Culture medium and induction method for improving saffron callus induction rate
A callus induction and culture medium technology, applied in the field of plant tissue culture, can solve the problems affecting the fast propagation efficiency of saffron tissue culture, waste of explants, low induction rate of saffron, etc., so as to promote the induction of saffron callus, promote the The effect of dedifferentiation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0016] Embodiment 1: Preparation of a culture medium for improving the induction rate of saffron callus.
[0017] According to the MS medium composition and consumption shown in Table 1 and the medium composition and consumption of improving the Saffron callus induction rate shown in Table 2, prepare the medium for improving the saffron callus induction rate of the present invention.
[0018] Use a balance to weigh the components in the MS medium, PAA (phenylacetic acid), 6-BA (6-benzyl adenine), banana puree, sucrose and agar powder, put them in a triangular flask, add an appropriate amount of distilled water, and stir to dissolve , and adjust the pH to 6.0 with HCL and KOH, and set the volume to 1000 mL. Seal the flask, place it in an autoclave, and sterilize it at 121°C for 20 minutes, then place it in an ultra-clean workbench to cool naturally, and set it aside.
[0019] When cooled to 50-60°C, divide the culture medium into tissue culture bottles, let it cool in the air,...
Embodiment 2
[0024] Embodiment two: Saffron corm induction culture.
[0025] Prepare the medium for improving the saffron callus induction rate by the method described in Example 1, and set aside.
[0026] Take fresh and healthy saffron bulbs that were born in the current year as explants, place them in a refrigerator at -4°C for 48 hours of vernalization at low temperature, then take out the bulbs and rinse them with water, dry the surface water with filter paper, and set aside.
[0027] Shake and soak the bulblet obtained above with 75% alcohol for 30 seconds, take out the bulblet, rinse it with distilled water for 3 times, and then use 1% HgCl 2 Soak for 4 minutes, then take out the small bulbs, rinse them with distilled water for 3 times, then soak them in 10mg / LPAA (phenylacetic acid) solution for 5 minutes, take out the small bulbs, and set aside.
[0028] The bulblet of above-mentioned gained is cut into the fritter of 0.5-1 centimeter with sterile scalpel, and inoculate in the cul...
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