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Blots were quantitated using ImageJ software (NIH) or iBright Analysis software.
The Northern blots were quantitated using ImageQuant v1.2 and the ratios of induced FLO11, relative to ACT1 internal control RNA were thus obtained.
Blots were quantitated using Gel-Pro (MediaCybernetics, Silver Spring, MD).
Where indicated, western blots were quantitated using ImageJ software.
The blots were quantitated using the Biometra BioDocAnalyze 2.0 software (Biometra, Göttingen, Germany).
All western blots were quantitated using ImageJ (National Institutes of Health) densitometry software.
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Signal intensity of Western blots was quantitated using a PhosphoImager (Kodak, Rochester, NY, USA).
Hybridization signals from a representative Northern blot were quantitated using ImageJ (NIH) and normalized to 18S rRNA levels.
Western blot signals were quantitated using VersaDoc (Biorad).
Western blot images were quantitated using the Odyssey Infrared Imaging System software.
Protein band intensities from western blot analyses were quantitated using the Quantity One 1D analysis software v.4.6.0 (Bio-Rad).
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