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For quantification, bands were analysed using ImageJ (NIH, Bethesda, MD, USA) and presented as a ratio to β-actin.
For quantification, bands were analyzed by ImageJ 1.46 (ref. 57) and the Odyssey imaging software (LI-COR Biosciences).
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For quantification, band intensity was measured using the NIH ImageJ program.
All of the membranes were analyzed by scanning densitometry and the quantification of bands was normalized using internal standards for each band.
Bands were visualized using an enhanced chemiluminescense detection kit (Pierce Co .. Quantification of bands was done by gel densitometry with gel image analysis system (American UVP Co).
(E ) Fluorescence quantification of bands at 90, 50, and 43 kDa demonstrating saturation of the 43 kDa band, but not the 90 or 50 kDa bands.
Graph shows quantification of bands by densitometry (n = 3), calculated as the ratio in Optical Density between the bands corresponding to RpoS and DnaK.
Quantification of bands was performed using Image J software.
Quantification of bands were performed by using ImageJ and normalized with β−tubulin levels.
Quantification of bands were performed by using ImageJ and normalized with histone H3 levels.
Quantification of bands was carried out with Chemi imager™ using the AlphaEase software (Alpha Innotech, CA).
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