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The ammonia concentration in the effluent stream was monitored with the thermal conductivity detector and the area under the peak was integrated using the software GRAMS/32 to determine the amount of desorbed ammonia.
For overlay-images the signal of the 19F peak was integrated and afterwards the dataset was zero-filled to a matrix of 200×200×16 pixels.
Each individual peak was integrated and then normalized.
Area of the first peak was integrated after baseline correction from the time of LPS stimulation to the first minimum for each cell using Matlab function trapz.
After performing Fourier transformation and making phase and baseline corrections, each H peak was integrated using 1D WINNMR software (Bruker Biospin).
The area of each peak was integrated to facilitate a comparison of secondary metabolite production within an investigated factor but not between plant species.
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All peaks are integrated and the integrals are recorded in a spreadsheet.
Peaks were integrated individually and the total integrated peak area of each spectrum normalized to 10000.
Eluents were detected by a variable wavelength ultraviolet (UV) detector at 340 nm, and peaks were integrated by using a HP3395 integrator.
The HPLC peaks were integrated and the concentrations in sample solutions were calculated.
Peaks were integrated and measured against a standard calibration curve.
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