T
Tej
@scienthusiast.bsky.social
Proteomics, Mass Spectrometry
82 followers77 following162 posts
Universally SDS performs good> additional lysis of pellet and sup+pellet lysate is more comprehensive> Urea has bias to nuclear proteins...and Fig 4 is cool. Although, it is a bit alarming to see the amount of proteins being left out in the pellet.. dual lysis is the way to go?
Lysis buffer selection guidance for mass spectrometry-based global proteomics including studies on the intersection of signal transduction and metabolism https://www.biorxiv.org/content/10.1101/2024.02.19.580971v1
Lysis buffer selection guidance for mass spectrometry-based global proteomics including studies on the intersection of signal transduction and metabolism https://www.biorxiv.org/content/10.1101/2024.02.19.580971v1
Prerequisite for a successful proteomics experiment is a high-quality lysis of the sample of interes
T
Tej
@scienthusiast.bsky.social
Proteomics, Mass Spectrometry
82 followers77 following162 posts