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The mass spectrometer operated for quantitative analysis in full scan MS/MS and quantitation was based on post processing MRM extracted ion chromatograms.
Quantitation was based on a gallic acid standard calibration curve.
Quantitation was based on a procyanidin B-2 standard calibration curve, and results are reported as mg/g of total flavanols per gram of sample for fruit powders and mg per serving for fruit products.
Quantitation was based on a trolox (6-hydroxy,2,5,7,8-tetramethylchroman-2-carboxylic acid) standard calibration curve, and results are reported as μm trolox equivalents per gram of sample for fruit powders and μm trolox equivalents per serving for fruit products.
Quantitation was based on phosphorimage analysis (Fujix BAS2000 or Fujifilm FLA-5100).
Quantitation was based on comparisons to internal standard DNA containing a known amount of AP sites.
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Quantitation is based on a spectral fit that uses previously determined infrared molecular line parameters generated in our laboratory, including line positions, line strengths and nitrogen-broadened half-widths for these species.
Raw instrument data was extracted and then processed through Metabolon in-house developed peak detection and integration software (quantitation is based on area under the curve from MS data).
Peptide quantitation is based on MS signal intensities of individual LC-MS analyses.
Quantitation is based on phosphorimage analysis (Typhoon 9400; GE Healthcare).
In the analog methods, standard curves are necessary for quantitation, because the quantitation is based on an assay signal, or output, not counting.
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