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Unlabeled extracts were mixed with a C metabolite library, and compounds were quantified using the FMQ(1) and corrected ITOCSY protocols.
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The inhibitory effects of compounds were quantified using MTT assay.
The absolute amounts of compounds were quantified using GCsolution Postrun (Shimadzu Corporation) with automatic peak detection and noise measurement.
Compounds were quantified using a standard calibration curve.
Compounds were quantified using gas chromatography with electron capture and mass spectrometry detection.
Inorganic ionic compounds were quantified using an ion chromatograph following standard methodology for airborne particulate matter.
Individual volatile compound peaks were quantified using the combined peak area of two specific and abundant ion traces per compound using MS Work Station Data Analysis software (Varian) and normalized by the 104 + 132 ion trace peak area from tetralin in each sample.
Components for which standards were not available were quantified using the standard curve of a related compound.
The bands were quantified using the Odyssey quantifying software.
DNAs were quantified using the Nanodrop spectrophotometer.
Proteins were quantified using the Bradford Assay.
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