FPbase

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FPbase

@FPbase

The Fluorescent Protein Database. tweets by @TalleyJLambert

शामिल हुए Ocak 2019
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FPbase
FPbase@FPbase·
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 fpbase.org/spectra
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FPbase
FPbase@FPbase·
@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 x.com/FPbase/status/…
FPbase@FPbase

@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: fpbase.org/protein/mstayg… - Ivorra-Molla et al is "StayGold-E138D": fpbase.org/protein/staygo… - Piatkevich et al is mBaoJin fpbase.org/protein/mbaoji…

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Joachim Goedhart
Joachim Goedhart@joachimgoedhart·
Carefully read this thread (and cited references!!) before choosing between mStayGold, mStayGold, and mStayGold x.com/christlet/stat…
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James Manton
James Manton@JamesDManton·
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.
James Manton tweet media
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FPbase
FPbase@FPbase·
recently hit 2,000,000 sessions on @FPbase ! 📈
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Ivan Maslov
Ivan Maslov@IvanMasl0v·
Mutagenesis of #FbFP #LOV domain: 🟠 22 variants with 486-512 nm emission maxima 🟠 three-channel imaging via spectral unmixing 🟠 two-channel fluorescence lifetime unmixing doi.org/10.1101/2022.1… Congratulations, @ivangushchin, @Aynya5, and all the authors! @FPbase
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FPbase
FPbase@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!
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Christopher A. Baker
Christopher A. Baker@bakermind·
Back in the day there was this person at Cornell who published a bunch of two-photon cross sections for fluorophores, and then there was a legendary paper from University of Montana that measured a bunch of RFPs, but I'm still longing for an @FPbase for 2P absorption
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Ben Campbell
Ben Campbell@lysergicdesigns·
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! 🧵nature.com/articles/s4159…
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FPbase
FPbase@FPbase·
@mycroscopy Wow, that’s a really impressive amount of organization! Very cool, congrats
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Elnaz Fazeli
Elnaz Fazeli@mycroscopy·
Nice to know the time we spent making these setups haven’t gone to waste. You can find all the @fpbase microsopes we made here: #content/view/193954699" target="_blank" rel="nofollow noopener">wiki.helsinki.fi/plugins/servle… Just click on each instrument and scroll down to see the fpbase link for it.
andrey a@aandr314

this is genius: @helsinkiuni BioImaging Unit utilizes @FPbase to allow users test their fluorophores fpbase.org/microscope/u4g… cc @Daniel_Wa19

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FPbase
FPbase@FPbase·
anyone out there routinely express FPs in Chlamydomonas? any modern suggestions for SNR? (presumably red, but any expression gotchas?)
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FPbase@FPbase·
@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 :)
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