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Enzymatic assay for recombinant human HNMT An enzyme solution (0.1 M TrisHCl buffer [pH 7.4] containing 10 nM rhHNMT [Novus Biologicals, Centennial, CO, USA] and 0.4 mg/mL BSA) and substrate solution (0.1 M TrisHCl buffer [pH 7.4] containing 10 M histamine and 10 M SAM with or without ERGO) were separately preincubated at 37 C for 5 min, and 25 L of each solution was mixed together

Their ferroptosis inhibition is mediated by regular antioxidant pathways (ROS scavenging and iron chelation), rather than the redox-based catalytic recycling pathway by FER-1 514

SchapiraAHCooperJMDexterDClarkJBJennerPMarsdenCD.Mitochondrial complex I deficiency in Parkinsons disease

It plays a crucial role in transporting fatty acids into mitochondria to produce adenosine triphosphate (ATD), which is vital for energy production in skeletal muscle and heart