Affinity-purification mass spectrometry (AP-MS) is the preeminent technique for identification of eukaryotic protein complexes in vivo. AP-MS workflows typically express epitope-tagged bait proteins,
GOLM1 Interactome proteome raw data files and GOLM1 liver snRNA seq raw data used for uMAP for the publication of: Insight into the function of GOLM1 in cholangiocytes through interactomics analysi
Output file from Xevo G2-XS Quadrupole Time-of-Flight (QToF) mass spectrometer with Ubiquitin-green fluorescent protein containing incorporated O-methyl-L-tyrosine
Protein scores of >29 was calculated for the 5% confidence threshold.MALDITOF MS/MS sequence results of the 70 kDa band detected in the supernatant of regenerated protoplasts of R. oryzae grown in the