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Single-application packs were packed in bags of 20 and marked with a label plate.
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Detection devices: Numerous multi-label plate readers enable a wide range of plate-based assays.
Fluorescence was then measured using the Enspire multi-label plate reader (Perkin Elmer).
Luminescent signal was measured by Perkin Elmer Envision 2102 multi-label plate reader.
Assessment of the cell growth after 72, 96, and 120 hr of treatment was carried out by the Cell-Titer Glo luminescence assay (Promega) in an Envision Multi-label plate reader (Perkin-Elmer, Waltham, Massachusetts).
The redox dye, resazurin (Sigma), was added to cells 13.5 h after treatment and incubated with cells for 1.5 h before reading fluorescence signal on a multi-label plate reader (EnVision® PerkinElmer).
Fluorescence anisotropy was measured using a Victor 3V (Perkin Elmer) multi-label plate reader.
Plates were read with a Perkin Elmer Envision multi-label plate reader.
The intensity of the color change was measured spectrophotometrically with Victor™ X4 multi-label plate reader at the wave length of 450 nm.
Immediately, we read absorbance of each well on Victor™ X4 multi-label plate reader at the wave length of 450 nm.
The reaction was stopped with 1 M HCl, and absorbance was read at A450nm using a 1420 multi-label plate reader (VICTOR3 TM V, PerkinElmer).
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