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CMV quantification was done by densitometry analysis using ImageQuant 5.2 (Molecular Dynamics, GE Healthcare).
Band intensity was measured by densitometry analysis using a Fotodyne Digital Imaging system and TotalLab v2005 software.
Differences in protein bands were determined by densitometry analysis using the Kodak 1D Image Analysis Software and Kodak films developed on the Hope micro-max developer.
To determine relative protein amounts, three representative exposures for each sample were quantitated by densitometry analysis using the ImageJ free software.
Band intensities were quantified by densitometry analysis using Bio1D software (Vilber Lourmat, Marne La Vallée, France).
Semi-quantification was made by densitometry analysis using Image J software (NIH).
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Immunoblots were quantified by band densitometry analysis using GeneTools™ software.
Amount of M2e protein incorporated in M2e VLP was calculated by spot densitometry analysis using serial diluted rM2e protein as a standard as shown in Figure 1(f) using Western blotting as described [ 19].
Semi-quantitative analysis of ELP3 and β-actin protein levels was carried out by scanning of western blots and densitometry analysis using Scion Image or ImageQuant software.
Western blots were subjected to densitometry analysis using ImageJ software.
Images captured with Image Studio Lite 5.0, and ImageJ 1.49o (NIH) software were used to quantify changes in protein expression by densitometry analysis and using β-actin (soluble fraction) as the loading control.
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by spectrophotometric analysis using
by multivariate analysis using
by numerical analysis using
by corresponding analysis using
by bioinformatic analysis using
by western analysis using
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by elemental analysis using
by densitometric analysis using
by biochemical analysis using
by gravimetric analysis using
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by hydrodynamic analysis using
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