Cultivation method for producing hupenine A through in vitro induction proliferation of thallus of huperzia serrata
A technology of Huperzia serrata and Huperzine A, applied in the field of induction and proliferation of isolated Huperzia serrata fronds, can solve the problems of lack of natural Melaleuca pagoda resources, large supply gap of Hup-A, and high cost
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Select robust and pest-free wild Huperus serrata plants, and take new branches about 3cm long that were pumped out in the same year;
[0025] After washing off the dust on the branches and leaves with tap water, soak them in detergent liquid for 6-10 minutes, then brush the branches and leaves with a soft brush, rinse them in tap water, absorb the water droplets with filter paper, and put them into a sterile container for surface cleaning. Sterilization treatment: transfer to the ultra-clean workbench, then sterilize with 75% ethanol for 0.5min--1min, wash with sterile water, blot the water, and then sterilize with 0.1%-0.5% HgCl 2 Add 1 drop of Tween 80 to soak the disinfection material for 6-10 minutes, pour off the liquid medicine, and rinse with sterile water for 6-8 times. Then, under sterile conditions, the new shoots of Huperz serrata were cut into stem segments with a length of about 0.5-1 cm, and inoculated on the prepared thallus differentiation starting med...
Embodiment 2
[0035] Select healthy and pest-free wild Huperzia serrata plants, take the new shoots about 3cm long that were pumped out in the same year, and after cleaning and disinfecting the explants, under aseptic conditions, cut the new shoots of Huperzia serrata into small stems with a length of about 0.5-1cm. Inoculate on the prepared thallus differentiation priming medium and culture. (1) Phalloid differentiation initiation medium: 1 / 2 (6,7-V)+IAA0.5mg / L (units the same below); (2) Phalloid subculture proliferation medium: 6,7-V +NAA0.5, sucrose consumption 20g / L, other are identical with embodiment 1.
Embodiment 3
[0037](1) Phalloid differentiation initiation medium: 1 / 2 (6,7-V)+IAA1.0mg / L (the unit is the same below); (2) Phalloid subculture proliferation medium: 6,7-V +NAA1.0, sucrose consumption 25g / L, other are identical with embodiment 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