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To determine the binding kinetics and affinity, we performed SPR experiments, where concentration series of the QMP-engineered albumin variants were injected over immobilized human FcRn at pH 5.5 (Fig

It promotes the conversion of liver glycogen to glucose and increases gluconeogenesis, as well as enhancing fat breakdown to provide energy

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Oncol Lett (2018) 15(4):547380

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