Applications of conjugated polymer pfp-g2
A technology of polymers and microorganisms, applied in the field of chemistry, to achieve the effect of regular size
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0049] Embodiment 1, growth and luminescence curve of Vibrio harveyi
[0050] (1), recovery culture of Vibrio harveyi
[0051] Using Vibrio harveyi BB170 as a template, use 75% alcohol absorbent cotton to sterilize the outer surface of the purchased ampule bottle containing Vibrio harveyi BB170 in an ultra-clean workbench, heat the top of it with a flame, and drop 300-400 μL of sterile Water to the top of the heated ampoule to rupture it. Draw 300-500 μL of suitable liquid culture medium (can be replaced by sterile water), drop it into the ampoule bottle, shake and blow lightly, so that the freeze-dried bacteria dissolve and form a suspension, absorb all the bacterial suspension, and transplant them into two 2216 cells respectively. In the solid medium of marine bacteria, culture at 30°C for 24 hours. Use an inoculation loop to scrape an appropriate amount of thalli to inoculate into the new 2216 marine bacteria solid medium, and continue to cultivate at 30°C, so that the co...
Embodiment 2
[0058] Example 2. Imaging experiment of Escherichia coli MG1655 and conjugated polymer PFP-G2
[0059] (1), recovery culture of Escherichia coli
[0060] Taking Escherichia coli MG1655 as an example, use 75% alcohol absorbent cotton to sterilize the outer surface of the purchased ampoule containing Escherichia coli MG1655 in the ultra-clean workbench, heat the top of it with a flame, and drop 300-400 μL of sterile water into the heated The tip of the ampoule was broken. Draw 300-500 μL of suitable liquid culture medium (can be replaced by sterile water), drop it into the ampoule, gently shake and blow it, so that the freeze-dried bacteria dissolve into a suspension, absorb all the bacterial suspension, and transplant it into two LB solids In the culture medium, culture at 37° C. at 180 rpm for 12 hours. Use an inoculation loop to scrape an appropriate amount of bacterium and inoculate it into a new LB solid medium, rotate at 180rpm at 37°C and continue to cultivate, so that ...
Embodiment 3
[0066] Example 3, the influence of the PFP-G2 polymer shown in formula I on the signal molecule shown in formula II in Escherichia coli MG1655
[0067] (1), recovery culture of Escherichia coli MG1655
[0068] With the step (1) of embodiment 2.
[0069] (two), the synthesis of PFP-G2 polymer shown in formula I
[0070] With the step (2) of embodiment 2.
[0071] (3), the compound PFP-G2 polymer shown in formula I is introduced in Escherichia coli MG1655
[0072] Pick an appropriate amount of Escherichia coli MG1655 from LB solid medium and place it in LB liquid medium, culture it with shaking at 180rpm at 37°C for 5-10h, adjust the OD with LB medium 600 The value is 1.0. Take a small amount of bacterial solution and dilute it 1000 times with LB medium, add PFP-G2 polymer shown in formula I with a final concentration of 100 μM, and control group does not add PFP-G2. Shake culture at 37°C at 180rpm for 1-8h, and the bacteria The solution was centrifuged at room temperature ...
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