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Measuring protein turnover is essential for understanding cellular biological processes and advancing drug discovery. The multiplex-DIA mass spectrometry (DIA-MS) approach, combined with dynamic SILAC labeling (pulse-SILAC, or pSILAC), has proven to be a reliable method for analyzing protein turnove...
ORGANISM(S): Homo sapiens (Human) 
2025-05-14 | PXD057632 | Pride
This projetc provides tandem mass spectrometry datasets of mixtures of specific fractions from microbial isolates enabling multiplex proteotyping without labeling. A mixture of eleven fractions and a mixture of twenty-one fractions respectively were prepared and analyzed in a single nanoLC-MS/MS run...
ORGANISM(S): Stenotrophomonas maltophilia Serratia marcescens Pseudopedobacter saltans Methylorubrum extorquens Kineococcus radiotolerans Microbacterium oxydans Ralstonia pickettii Sagittula stellata Sphingomonas yabuuchiae 
2025-09-15 | PXD035870 | Pride
We developed a multiplex pseudo-isobaric dimethyl labeling (m-pIDL) method for proteome quantification to extend the capacity of the fragment ion-based method to 6-plex by one-step dimethyl labeling with several millidalton and dalton mass differences between precursor ions and enlarging the isolati...
ORGANISM(S): Homo Sapiens Escherichia Coli 
2019-01-22 | PXD012457 |
Aptamer-Based Proteomics Measuring Preoperative Cerebrospinal Fluid Protein Alterations Associated with Postoperative Delirium
Digital proteomics by DNA sequencing
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