May I present to you my agar art of the structure of green fluorescent protein (GFP), painted with bacteria genetically engineered to express the protein! #meta

Thanks Sebastian S. Cocioba🪄🌷 for the E. coli and Nick Coleman for the super bright free use GFP! #fuGFP #SciArt

Overnight nanopore sequencing service.... roarsome!🦕 #plasmids #microbes #amplicons plasmidsaurus

If you've been using one of our Oxford University dropboxes, you may have spotted something unusual...!!!🦖🚲

Daily pickups at Dunn_School (and @DunnSchool.bsky.social), Oxford Biology, Centre for Human Genetics, and Old Road Campus Research.

Huge shoutout to Dr Malcolm Sim, Malcolm Sim!

Need to outsource some mouse experiments, ideally LA or SD. Any recommendations?

🐁🐁🐁

Anthony Berndt Kelvin Lau always @klausenhauser on ☁️ 🪡 🐘 Primordium Primordium employee here - hearing that we were able to help made my day :)

Pretty sure we have the fastest and most innovative lab automation team in history at plasmidsaurus 🦖🦕🧬🤖

There is nothing more fun than working with a team of high-agency top performers to unlock new capabilities that others claim are impossible.

This team rocks! 🦾

Thanks to Mark Budde and other alum for hosting a great beer chat! Grateful to have continued connections and proud of his success!

Great to be back in Seattle.

I'm struggling to wrap my head around the new Weissman lab myHSC depletion paper: nature.com/articles/s4158…
The first authors don't seem to be on twitter but hoping I can crowdsource a fun discussion. Daniel Bryan Goodman Michal Tal, PhD Jeffrey Mold Ansu Satpathy Caleb Lareau...

Just. Share. Your. Plasmids.

Enough with the MTAs. It's the age of synthesis. The material doesn't matter and all you are really doing is saving your peers time and money. The thing, once constructed, is an infinitely renewable resource. Just share it.

Don't be weird.

I'll be in Seattle this weekend, who's around?

Terraform's vision is our best bet at a sustainable energy future.

here’s the CEO of Cognition

while you were partying, he was studying the blade

plasmidsaurus I honestly have you guys sequence EVERYTHING before I use it now - even stuff I pull out of my own freezer.

Amazing how much stuff from my own freezer has had duplications...

Anthony Berndt I hate applying it to everything but surely it's an 80:20 rule situation right? 80% of your cloning goes smoothly and only requires 20% of your effort, but that pesky fraction of cloning experiments that don't work the first time are always tough to get working

Beautiful rainbow in South San Francisco. 🌈

Oh... so that's why my LR reactions aren't working. Thanks plasmidsaurus 🙄😶😓

An example of a 2D projection of single cell data. Cells are colored by fluorescent protein reporters indicating clone of origin. X axis is physical distance in X. Y axis is physical distance in Y. What does it mean?

Got a plasmid backbone that frankensteined the AmpR promoter with a weirdly codon reoptimized KanR. Only the promoter was annotated on the supplied map.

Could not figure out why I was getting zero clones post ligation or gibson assembly for a week because I was Amp selecting