We attached the photoclick moiety to proteins in RPE1 cells 🧫 and used a DMD projector from @EKBTechnologies on a @healthcare.nikon.com Ti2🔬 to selectively irradiate regions.
Activated areas are labeled w fluorophores✨ -we even printed the @rsc.org logo!
2/🧵
We attached the photoclick moiety to proteins in RPE1 cells 🧫 and used a DMD projector from @EKBTechnologies on a @healthcare.nikon.com Ti2🔬 to selectively irradiate regions.
Activated areas are labeled w fluorophores✨ -we even printed the @rsc.org logo!
2/🧵
We have awesome news for you! All our 6 SPY-DNA probes work beautifully well with the U-ExM protocol.
You can now tune the color of the DNA channel to your needs, according to the fluorophores on your preferred antibodies.
spirochrome.com/products/?_c...
We have awesome news for you! All our 6 SPY-DNA probes work beautifully well with the U-ExM protocol.
You can now tune the color of the DNA channel to your needs, according to the fluorophores on your preferred antibodies.
spirochrome.com/products/?_c...
#chemistry #openaccess #science
#chemistry #openaccess #science
Our front cover this week features Georgina K. Such, Chris Ritchie et al 🤩
'Monitoring structural change and drug release of responsive nanoparticles using polarity-sensitive fluorophores'
🔗 doi.org/10.1039/D5SC...
Our front cover this week features Georgina K. Such, Chris Ritchie et al 🤩
'Monitoring structural change and drug release of responsive nanoparticles using polarity-sensitive fluorophores'
🔗 doi.org/10.1039/D5SC...
👉doi.org/10.1039/D5TC...
👉doi.org/10.1039/D5TC...
Fluorescence minus one (FMO) answers the right question:
Where does the true negative population fall once all other fluorophores are present?
(6/n)
Fluorescence minus one (FMO) answers the right question:
Where does the true negative population fall once all other fluorophores are present?
(6/n)
Apply here- bit.ly/49YQl7q
Apply here- bit.ly/49YQl7q
Open-access article: doi.org/10.1530/JOE-25-0253
Open-access article: doi.org/10.1530/JOE-25-0253
• Always check actual emission filters for your machine, not generic vendor diagrams
• Use a spectral viewer for your specific cytometer
• Place bright fluorophores on low-expression markers (and vice versa)
• Use FMOs (fluorescence-minus-one controls) to verify gating
(4/5)
• Always check actual emission filters for your machine, not generic vendor diagrams
• Use a spectral viewer for your specific cytometer
• Place bright fluorophores on low-expression markers (and vice versa)
• Use FMOs (fluorescence-minus-one controls) to verify gating
(4/5)
“Two fluorophores look similar on the map—that must mean I can’t use them”
(or the opposite…)
“They have different names, so it must be fine”
(2/5)
“Two fluorophores look similar on the map—that must mean I can’t use them”
(or the opposite…)
“They have different names, so it must be fine”
(2/5)
🔗doi.org/10.1039/D5MA...
🔗doi.org/10.1039/D5MA...
Check out "Construction and optimization of organic fluorophores in NIR-II fluorescence imaging" by Xiaozhen Li, Yanlong Yang, Ruohan Zhang and Wei Huang
Read the full review here 👇
Check out "Construction and optimization of organic fluorophores in NIR-II fluorescence imaging" by Xiaozhen Li, Yanlong Yang, Ruohan Zhang and Wei Huang
Read the full review here 👇
D-CHAB @ethz.ch
www.nature.com/articles/s41...
D-CHAB @ethz.ch
www.nature.com/articles/s41...
->Nature | More from Lil Dr Glen EcoChat at BigEarthData.ai