Try the new FPbase spectra viewer!
Completely rewritten to be faster, more customizable, and full-featured:
• SVG/PNG/CSV export
• state recovery & URL sharing
• keyboard shortcuts for rapid entry 💚
• efficiency calculations
• full documentation
https://t.co/sG8FQHD0ye
@joachimgoedhart@facette_lab@weinberz also commented in the thread by @christlet... but just an update that the names on FPbase have been updated keeping the conventions proposed in this thread here. With "mStayGold" (from Ando et al), StayGold-E138D, and mBaoJin
https://t.co/MnC46FuIUJ
@weinberz@joachimgoedhart@christlet Thanks @christlet for the helpful thread!
An update on the FPbase namings:
- "mStayGold" now refers to QC2-6 FIQ from Ando et al: https://t.co/JmMi1AAjJM
- Ivorra-Molla et al is "StayGold-E138D": https://t.co/sbzJxsm4Z0
- Piatkevich et al is mBaoJin https://t.co/kUqTm968af
@weinberz@joachimgoedhart@christlet Thanks @christlet for the helpful thread!
An update on the FPbase namings:
- "mStayGold" now refers to QC2-6 FIQ from Ando et al: https://t.co/JmMi1AAjJM
- Ivorra-Molla et al is "StayGold-E138D": https://t.co/sbzJxsm4Z0
- Piatkevich et al is mBaoJin https://t.co/kUqTm968af
This exercise was less informative than I'd hoped, but perhaps it's interesting to someone else: spectroscopically-inferred estimates of densities of states for a selection of fluorescent proteins spanning the visible spectrum. Data from @FPbase.
Mutagenesis of #FbFP#LOV domain:
🟠 22 variants with 486-512 nm emission maxima
🟠 three-channel imaging via spectral unmixing
🟠 two-channel fluorescence lifetime unmixing
https://t.co/5Kgc045vlh
Congratulations, @ivangushchin, @Aynya5, and all the authors!
@FPbase
@bakermind took a look, there are 90 2P spectra currently available in the database. So, this is a user interface problem rather than a data storage problem 😬 ... (GM units are also stored in the database, but easily accessible) my apologies!
Our article reporting hyperfolder YFP (#hfYFP) and other fixative-resistant fluorescent proteins based on #mGreenLantern is now available at @naturemethods. hfYFP enhances electron- and expansion-microscopies, protein purification, and so much more! 🧵https://t.co/hyUvgeno85
Happy to share the Methods in Molecular Biology issue on Fluorescent Proteins 🌈🎉😀. Including many “much awaited” protocols on and about Fluorescent Proteins/applications. A big THANKS to authors across the globe for contributing. 👏🏻💐
https://t.co/0yCqaDfzKw
@beniroquai That would be 50% of max Extinction coefficient (not QE). If you’re asking whether it “works”, it will be case-specific. Will require more illum power, so more damaging to sample. And may generate more background, depending on sample. But with enough power you’ll get photons :)