Method for culturing scindapsus aureus through terminal bud
A technology for terminal buds and green dill, which is applied in the field of using terminal buds to cultivate green dill, can solve the problems of large amount of cuttings, affecting reproduction rate, and wide area, and achieves the effect of shortening the production cycle.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0041] Step 1, selection of explants. Specifically, select a strong mother plant with normal shape and vigorous growth for pretreatment (use 80% carbendazim wettable powder 1000 times liquid to irrigate the roots, once every 10 days), cut off the 5 cm stem section terminal bud at the stem growth point, and remove it from the surface. Miscellaneous and cleaned explants were transferred to the ultra-clean workbench for disinfection treatment. This disinfection was first soaked in alcohol with a volume fraction of 75% for 15 seconds, and then soaked in 0.1wt% HgCl solution for 13 minutes. After washing with bacterial water for 3 to 5 times, sterile pothos stems are obtained.
[0042] Step 2, induction culture of callus. Specifically, the stem section of the pothos is trimmed to a length of 2cm on the ultra-clean workbench and under sterile conditions, and inoculated into the callus induction medium (including 412.5mg / L ammonium nitrate, 475mg / L potassium nitrate, 110mg / L calciu...
Embodiment 2
[0052] Step 1, selection of explants. Specifically, select a strong mother plant with normal shape and vigorous growth for pretreatment (use 80% carbendazim wettable powder 1000 times liquid to irrigate the roots, once every 10 days), cut off the 8cm stem section terminal bud at the stem growth point, and remove it from the surface. Miscellaneous and cleaned explants were transferred to the ultra-clean workbench for disinfection treatment. This disinfection was first soaked in alcohol with a volume fraction of 75% for 15 seconds, and then soaked in 0.1wt% HgCl solution for 13 minutes. After washing with bacterial water for 3 to 5 times, sterile pothos stems are obtained.
[0053] Step 2, induction culture of callus. Specifically, the stem section of the pothos is trimmed to a length of 3 cm on the ultra-clean workbench and under sterile conditions, and inoculated into the callus induction medium (including 412.5 mg / L ammonium nitrate, 475 mg / L potassium nitrate, 110mg / L calc...
Embodiment 3
[0063] Step 1, selection of explants. Specifically, a strong mother plant with normal shape and vigorous growth is selected for pretreatment (use 80% carbendazim wettable powder 1000 times liquid to irrigate the roots, once every 10 days), and the 6.5cm stem section terminal bud at the stem growth point is cut out. After removing impurities and cleaning, the explants are transferred to the ultra-clean workbench for disinfection treatment. The disinfection is first soaked in alcohol with a volume fraction of 75% for 15 seconds, and then soaked in 0.1wt% HgCl solution for 13 minutes. Use after disinfection After washing with sterile water for 3 to 5 times, sterile pothos stems are obtained.
[0064] Step 2, induction culture of callus. Specifically, the stem section of the pothos is trimmed to a length of 2.5cm on the ultra-clean workbench and under sterile conditions, and inoculated into the callus induction medium (412.5mg / L ammonium nitrate, 475mg / L potassium nitrate, 110mg...
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