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Approximately 10 g of protein was loaded into a polyacrylamide gel

Extracted ion chromatograms (MS) of precursor masses representing the unmodified N-terminal peptide of TGF1 (m/z 768.5) and the modified N-terminal peptide (m/z 877.2) A of m/z 768.2769.2 from DMSO treated TGF1, B of m/z 768.2769.2 from SF treated TGF1, C of m/z 876.7877.7 DMSO treated TGF1 and D of m/z 876.7877.7 SF treated TGF1

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roGFP2 reduction/oxidation assay The coding region of roGFP2 64 was cloned into the E.coli expression vector pDEST17, allowing expression roGFP2 fused to a 6xHis-tag

A.Rosales-LeyceguiF.Gaxiola-RubioA.Moreno-OrtizJ

These non-edited approaches have been shown to provide reasonable estimates of GSH (Terpstra et al., 2005, Wijtenburg et al., 2019), with improved performance at very short TEs, due to having less time for both J-coupling related phase dispersion and T2 relaxation (Wijtenburg et al., 2019), thereby preserving signal-to-noise ratio (SNR)