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By attaching an acetyl group to the sulfur atom of cysteine within the glutathione tripeptide, SAG resists enzymatic degradation in the gastrointestinal tract, crosses cell membranes intact, and is then hydrolyzed intracellularly by cytoplasmic thioesterases to release free, bioactive GSH directly inside cells

The vial format on this page is intended for in-vitro and animal research workflows, including subcutaneous injection studies covered in our GHK-Cu dosing protocol guide

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