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Luminescence was quantified immediately using a multimode plate reader (Tecan M1000, Tecan iControl 1.6 software; Tecan Austria GmbH, Grödig, Austria).
After incubation at 30°C for 30 minutes, absorption at 600 nm was quantified using a multimode plate reader (Tecan M1000).
After 15 min incubation, cells were washed with warm PBS and 50 µl PBS was used for measurement of TMRM fluorescence using a multimode plate reader (Ex.: 545 nm; Em.: 580 nm; Tecan M1000).
The optical density (OD) was read at 595 nm using a multimode plate reader (Varioskan Flash, Thermo Scientific, USA).
An MTT assay was performed using a multimode plate reader (Beckman Coulter) as described in the proliferation and cell viability assay.
After 72 h, 100 μL of the PicaGene LT2.0 luminescence reagent (Toyo Inki, Tokyo, Japan) was added to the cells and the luciferase activities were analyzed using a Multimode Plate Reader (EnSpire, PerkinElmer), according to the manufacturer's protocol.
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Towards this end, we derive a reduced-order model using a multimode Galerkin procedure.
The buffeting response of the bridge is then evaluated in frequency domain using a multimode approach.
The spectrometer is fibre-coupled to the microscope using a multimode (non-polarization maintaining) fibre to neutralize any possible polarization sensitivity of the gratings.
Luminescence was quantitated using a multimode microplate reader (BMG Labtech).
The fluorescence was read (Ex/Em=535/587 nm) using a multimode microplate reader (TECAN Infinite M200).
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