@AmandaLSmythers This also depends on volume of sample and concentration of peptides. Pushing 10s of uL of dilute peptides over a trap column takes a long time and can potentially clog that trap column more quickly than a couple of uL of pre-desalted samples!
Looking for multiple Proteomics/Metabolomics Staff Scientists at Northwestern Proteomics. DM me or @NLKProteomics is you're interested. Competitive Salary, lots of cool instrumentation, great colleagues, what else do you want? #chemjobs#massspec
@MattWFoster @asmsnews Same issue... I've tried two things... 1) Incognito mode. That worked. 2) If you click on the "i" in the top left hand corner, you can get the Zoom join ID and password, then join through the zoom client.
We have compiled a list of all the great TDP presentations and workshops at the ASMS Reboot 2020. Go here for the list https://t.co/M0WTsxbuOQ #ASMS2020
@byu_sam@JeongKyowon @JohnRYatesIII Exactly. Sequencers have one job... "ATCG", and they're engineered to do that task quickly and efficiently. Proteomics in all its flavors uses the same tool (MS). MS has far too many parameters to fiddle with, coupled with robustness issues at maximum sensitivity.
I've been thinking... #naturalproduct#biosynthesis (& many other) figures are begging to be shown in action, so I made a totally fake, yet plausible, NRPS biosynthesis of "fakeomycin" feat. a Cy domain. I want more GIF figures in my life! #chemdraw#chemtwitter#scienceanimation