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To examine the incorporation of GSH-derived cysteine into downstream pathways, we used an inverse stable-isotope labelling approach 34,35

Moreover, full-length BPC157 or single-site alanine-mutated BPC157 was dissolved in HBS-EP Buffer (Cytiva) at concentrations ranging from 1.89 nM to 31.25 nM through serial 2-fold dilutions

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