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Luciferase expression was analysed by addition of luciferase substrate in luciferase assay buffer (0.25 M Glycyl-Glyin, 0.015 M KPO 4 , pH 7.8, 0.015 M MgSO 4 , 4 mM EGTA, pH 7.8, 1 mM DTT, 2 mM ATP, 0.07 mM Luciferin) using the Mithras LB 940 plate luminometer (Berthold Technologies)

However, no significant differences were observed in the mRNA levels of lipid synthesis-related molecules between the CKO and Gly groups, indicating that PRMT1 may be involved in regulating fatty acid transport and oxidation (Fig

& Lukashev, D

Jalkanen AL, Coleman SJ, Wilusz J

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Antioxidant vitamin supplementation prevents oxidative stress but does not enhance performance in young football athletes