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Readings were performed using a luminescence plate reader.
Luminescence was measured using a luminescence plate reader (BMG Labtech PHERAstar FS, Germany).
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Luciferase activity was measured at the plate reader, using a luminescence program with 1" integration time.
The plates were read using a luminescence reader (Tecan Infinite M1000).
Luminescence was measured using a luminescence reader (Molecular Devices), and normalized for protein concentration.
The plates were read in a luminescence plate reader (PerkinElmer).
Following the manufacturer's instruction of Mitochondrial ToxGlo Assay (Promega), the amount of ATP was measured by luminescence using a plate reader (Synergy HT, Biotek).
Translation of luciferase protein for each reaction was measured as luciferase activity, by recording luminescence using a POLARstar Optima plate reader (BMG LabTech) programmed to perform multiple reads on each sample at 1 s intervals for a total of approximately 2 min.
Different genotypes were processed in biological triplicates and luminescence was measured using a Chameleon plate reader (Hidex, Turku, Finland).
OD and luminescence were measured using a multiwell plate reader (Wallac Victor 1420 multilabel counter) at 4 minute intervals, with agitation (30 seconds, 2.0 mm orbital shake prior to measurement) for an hour and a half.
Luminescence was quantified immediately using a multimode plate reader (Tecan M1000, Tecan iControl 1.6 software; Tecan Austria GmbH, Grödig, Austria).
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