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To stop the reaction, stop buffer (340 mM NaCl, 20 mM EDTA, 4 mM EGTA, 50 g/mL RNase A, 100 g/mL glycogen, and 3 pg/mL Drosophila DNA) was added, followed by incubation for 3 min at 4 C and for 39 min at 37 C

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Conclusions This study establishes a novel and critical molecular mechanism for the pharmacological actions of BPC157, centered on the BPC157-FBXO22-BACH1 axis

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221 SIRT3 orchestrates the metabolism reprogramming via controlling the balance between cytosolic glycolytic metabolism and mitochondrial oxidative metabolism