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Fluorescence intensity values were quantified using Image-pro plus software.
All hybridization slides were scanned by GenePix 4100A scanner after appropriate washing, and the average pixel intensity values were quantified using GenePix Pro 4.1.
ADC values were quantified using the PC workstation mentioned above.
Values were quantified using serial dilutions of sodium nitrite.
The Ct values were quantified using ABI software and the standard curve.
Densitometric values were quantified using the QuantityOne analysis software (Bio-Rad), taking into account the relative size of each fragment.
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Reaction rates and intrinsic reactivity values are quantified using a thermo-gravimetric analyzer.
The deviation of model result from experimental values is quantified using the statistical parameter of root mean square (RMS) error, {text{RMS }} = sqrt {frac{{mathop sum nolimits left( {X_{text{e}} ; - ;X_{text{p}} } right)^{2} }}{N}} (17 where X e, X p and N are experimental data, predicted value and number of observations, respectively.
The fluorescence intensity value was quantified using Image-pro Plus program.
The results were analyzed and cycle threshold (Ct) values of transcripts were quantified using CFX manager software (Bio-Rad).
In addition to P-values, the results were quantified using odds ratios (ORs) with 95% confidence intervals (CIs).
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