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Densitometry of the bands was analysed using NIH ImageJ software.
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Visible and infrared spectral bands were analysed using "The Lineament Extraction and Stripes Statistic Analysis" (LESSA) software package to examine changes in the lineament features and stripe density fields caused by seismic activity.
The bands were analysed using the Quantity One™ Software (Bio-Rad, Hercules, CA, USA).
For quantification, bands were analysed using ImageJ (NIH, Bethesda, MD, USA) and presented as a ratio to β-actin.
The separated proteins were stained using EZBlue (Sigma) and the bands were analysed using Q uantity O ne 1-D analysis software (Bio-Rad).
The relative intensifies of protein bands were analysed using the densitometric analysis software Image Lab version 5.1 beta, using a Chemidoc MP Imaging System for acquisition (Bio-Rad Laboratories).
To quantify western blot band densitometry, the relevant specified bands were analysed using ChemiImager (Alpha Innotech Co .. T-test was used and P-values were determined by unconditional logistical regression analysis by using the general loglinear option of SPSS 9.1 software (SPSS, Chicago, IL).
Each recording was analysed using the MATLAB Ledalab toolbox.
Luciferase activity was analysed using Dual-Luciferase reporter assay kit (Promega).
The sample was analysed using ESI-MS and the trapped carbamate Gly-Phe product was confirmed.
Also, the compressive strength evolution was analysed using cubic specimens.
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