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Fluorescent dots were quantified using ImageJ software (NIH).
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Enhanced chemiluminescence (ECL) signal was digitally captured with LAS-3000 imaging system, and the intensity of the dots was quantified using Multi Gauge software (Fujifilm, Japan).
Raw signal of individual dots was quantified using Odyssey 3.03 and ImageStudio software (LI-COR Biosciences) and plotted against protein quantity (Fig. 3b).
The distances between the dots in axial and transverse directions were quantified using image analysis (software Cell-P).
Cytokine-expressing lymphocytes were quantified using Fluorescence FL4 versus Fluorescence FL2/anti-cytokine-PE dot plots.
p-eIF2 α and nuclear signals were quantified using Imaris software (Bitplane, Belfast, UK) and the dots-per-cell ratio was calculated.
Data were quantified using MetaXpress software.
All images were quantified using ImageJ (NIH).
NRF2 images were quantified using ImageJ.
FRET measurements were quantified using ImageJ (NIH).
Images were quantified using Image J software.
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