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In this study we used electrochemistry-based targeted metabolomics to gain insights into the mechanisms of action of escitalopram/citalopram focusing on a set of 31 metabolites from neurotransmitter-related pathways

To obtain cell surface proteome lists for T cell, CAR-T cell and TCR-T cell monocultures (grown in the absence of tumor cells), we applied a log 2 -transformed fold change cutoff with a 5% false discovery rate (FDR), defined by the retention of cytosolic and nuclear proteins, which should not be labeled by LaccID (Supplementary Fig

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