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Protein bands were quantitated by densitometry, and analysed using GeneTools software.
Individual protein bands were quantitated by densitometry.
Bands were quantitated by laser densitometry.
Protein bands were quantitated by densitometry, and the values were expressed relative to actin (control for loading and transfer).
For protein quantification, blots were scanned and protein bands were quantitated by densitometry, using the VersaDoc image analyzer and the Quantity One program (BioRad).
The proteins were visualized by chemiluminescence (UVP, Bio Spectrum, USA) and the densities of specific bands were quantitated by densitometry using (Image J 1.37 software, NIH, USA) [ 19].
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The intensity of the bands was quantitated by NIH image.
The intensity of bands was quantitated by densitometry using Quantity One software (Biorad) as previously [ 4].
Results from three independent experiments were analyzed by Western blot, and the intensity of the bands was quantitated by densitometry, using AlphaInnotech FluorChem® HD2 instrument (Alpha Innotech, San Leandro, CA, USA) and analyzed using alphaeasefc software, provided by the manufacturer.
Intensities of the respective band were quantitated by densitometric analysis using Image Studio 2.0.38 software (Li-cor Biosciences).
Protein bands were quantitated in vivo by densitometric analysis using image analysis software (CS Analyzer; ATTO, Tokyo, Japan).
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