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Compounds were quantified as equivalents of cyanidin-3-glucoside, kaempferol, or quercetin, depending on their core compounds.
The tentatively identified peaks were quantified as equivalents of the following standards: chlorogenic acid isomers as CHA, dicaffeoylquinic acid isomers, tricaffeoylquinic acid and its derivative as CA, 20-hydroxyecdysone as EC, and the flavonoid monoglycosides as IQ.
Proteins were quantified as above.
Absorbance was read at 750 nm, using a microplate reader, and quantified as Trolox equivalents (mM/mg wet mass).
Samples were quantified as genome equivalents per μl (geq/μl) by fitting the sample Cts to the standard curve using the AB7500 Fast System SDS Software Applied Biosystems™™).
Thus, the assay can quantify as few as 10 DNA copies, which would correspond to 0.67% amplifiable templates in a background of 5 ng genomic DNA (equivalent to 1,515 haploid copies total input).
The antioxidant capacity from the serum sample to prevent ABTS oxidation is compared with that by Trolox (a water-soluble tocopherol analog) and was quantified as molar Trolox equivalents.
Absorbance was read at 755 nm and phenolics quantified as gallic acid equivalents.
Exercise behavior was quantified as weekly metabolic equivalents of task (MET) spent on exercise activities.
The capacity of plasma to prevent oxidation of ABTS is compared with that of trolox and is quantified as molar trolox equivalents.
Dopaminergic drug use was quantified as the l-dopamine equivalent dose (LED) [ 39].
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