Raghava

174 posts

Raghava

Raghava

@Raghava_Bio

Fundamental Biologist and Electrophysiologist. Currently a Post-doc at University of Wisconsin-Madison

Wisconsin, USA शामिल हुए Mayıs 2019
260 फ़ॉलोइंग61 फ़ॉलोवर्स
tina kim
tina kim@tinakim_neuro·
I am so honored to have been selected as a shortlisted finalist in neuroscience for the 2026 Takeda Innovators in Science Award with @NaturePortfolio! I’m excited to participate in Nature’s career development programs, while building meaningful connections with my peer awardees (including my good friend and colleague, Ai Ing Lim @Princeton!). Read about the award and the other amazing shortlisted candidates here: nature.com/immersive/inno… linkedin.com/company/takeda… linkedin.com/company/nature…
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Raghava
Raghava@Raghava_Bio·
@prat_i_k Hi Pratik Raghava here from Ed's lab. Congratulations on your new paper
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Pratik Kumar
Pratik Kumar@prat_i_k·
If you want to build such modern reagents and like doing a bit of organic chemistry and some biology, do consider joining my lab (DyeCraftLab.com) at National Centre for Biological Sciences (NCBS) Paper link: lnkd.in/enGd7Q5M
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Pratik Kumar
Pratik Kumar@prat_i_k·
Our collaborative paper is online! We built two types of genetically targetable live-cell permeable fluorescent reagents: biotin for organelle purification, and JQ1 for chromatin manipulation! We found how to chose the right dye for building such multifunctional dyes
David Solecki (pronounced so_lets_ki 😉)@So_lets_kiLab70

When chemistry meets neurons! Just dropped in @PNASNews Our game-changing paper on multifunctional fluorescent ligands for intracellular labeling. Luke Lavis and Pratik Kumar @prat_i_k built the epic tools; we got to unleash them! @JasonVevea & team nailed biotin-HaloTag for mitochondrial magic. My lab rocked the JQ1 version to shuffle chromatin in LIVE cells. First collab win for our Neuronal Cell Biology Division with Janelia—more to come! #Science #Neuroscience #ChemBio #scicomm #Fluorescence #HaloTag

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Raghava
Raghava@Raghava_Bio·
@tinakim_neuro Congratulations on HHMI Freeman Hrabowski scholar funding 👏
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tina kim
tina kim@tinakim_neuro·
Happy to share the lab’s latest research tagging psychedelic-activated neurons in mice. See the post below from first author @jessie_muir for a tweeprint on the work. Thanks to wonderful collaborators @DEOlsonLab @LinTianPhD and to our reviewers/editor! science.org/doi/10.1126/sc…
Jessie Muir@jessie_muir

Excited to share the Kim Lab’s newest paper in @ScienceMagazine with Sophia Lin (twitterless) and @tinakim_neuro ! We look at circuit mechanisms of psychedelic action underlying therapeutic-like effects in the PFC. science.org/doi/10.1126/sc…

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tina kim
tina kim@tinakim_neuro·
And it’s out! Our lab’s very first paper is published today @naturemethods! Our calcium-activated split-TurboID (CaST) can biochemically tag activated neurons within 10 minutes, enabling a molecular handle on functionally relevant cell ensembles: tinyurl.com/ddyecxze
tina kim@tinakim_neuro

Excited to share the first paper from our lab! tinyurl.com/5n7fvwvh We engineered a new kind of time-gated calcium integrator, CaST, that can rapidly and non-invasively tag activated neurons in vivo with a small, biochemical handle. What makes this tool special and unique? 1/6

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Raghava
Raghava@Raghava_Bio·
@NeuroBill Thanks for your recommendations Bill, I would definitely consider DigitimerDS3 next, its looks great
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NeuroBill - neurobill.bsky.social
@Raghava_Bio Sorry for not getting back to you. I thought I already had. I've used an iso-flex a lot. On paper they are great, but for me, the best is digitimer. DS3. The DS4 is very nifty, but I love the DS2s and DS3s. K.I.S.S.
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Raghava
Raghava@Raghava_Bio·
@NeuroBill Hi Can you help in understanding what causes this weird stimulus artefact? I get this sometimes, changing polarity works but the amplitude decreases I am using ISO-Flex unit
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Raghava
Raghava@Raghava_Bio·
@NeuroBill Hi Bill, did you miss this tweet from me earlier? Thanks
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Raghava
Raghava@Raghava_Bio·
@NeuroBill Hi Bill I accidentally found the origin of the issue. I suspect the stimulus isolation unit (SIU) is the culprit here. These two traces are from the same cell 10s apart but with different SIUs. The graph on the right is a scaled version of the left one for better resolution
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Avishek Roy
Avishek Roy@Avishek92·
This was fun participating in the contest thanks to @NolwennCloarec for arranging this. I also take this moment to say thanks to @letelliermathi1, @ebazbadillo & Agata Nowacka for the guidance to single cell electroporation
Interdisciplinary Institute for Neuroscience 🧠@iins_bordeaux

#ThursdayPicture🖼️Electroporation of organotypic slices, immune staining, incubation, labelling with #NeuN, #DAPI and #GFP, epifluorescence imaging and processing... find out all about these techniques in "The venomous arthropods of CA1"! 🧪🔬 by @Avishek92 ⬇️Caption⬇️

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Raghava
Raghava@Raghava_Bio·
Two Indian-origin professors, Venkatesan Sundaresan and Savithramma Dinesh Kumar from @ucdavis elected to the NAS, both from plant biology
National Academy of Sciences@theNASciences

We are thrilled to announce the election of 120 members and 24 international members to the National Academy of Sciences in recognition of their distinguished and continued achievements in original research. Congratulations to our new #NASmembers and welcome to the Academy!

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Raghava
Raghava@Raghava_Bio·
It's called an exit seminar at UC Davis, no defense!
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Raghava
Raghava@Raghava_Bio·
@NeuroBill And those traces are AMPAR-only currents with NMDAR and GABA blocked by AP-V (50uM) and Picrotoxin (100uM), respectively.
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Raghava
Raghava@Raghava_Bio·
@NeuroBill I have been using Iso-Flex for close to a decade but have yet to have this problem. This is due to the capacitive transients generated by the SIU. The unit I am using is a brand-new one with all-new batteries! Any suggestions?
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