Archaeol was quantified in samples obtained from four lactating cows with rumen cannulae that grazed on either white clover (WC) or perennial ryegrass (PRG) in a changeover design study with three 3-week periods.
Afterward, at each scoring date every 2 wk, milk SCC was quantified in samples from all mammary quarters and microbiologic culture was only performed on milk samples with SCC >200,000 cells/mL for multiparous cows and SCC >100,000 cells/mL for primiparous cows.
DNA concentration was quantified in samples prior to genotyping by using Quant-iT PicoGreen dsDNA Reagent (Invitrogen, Eugene, OR, USA).
As for samples freshly cultivated, 106 to 107 CFU/ml were quantified in samples of P. aeruginosa stored 3 weeks in mineral water, indicating that there was no increase or decrease of the population after storage.
Apoptosis of glomerular cells was quantified in samples submitted to detection of the M30 cytodeath marker.
Serum HBV DNA, HBeAg, and HBsAg were quantified in samples taken at baseline, during treatment, and during 6 months of off-treatment follow-up.
Serum haptoglobin was quantified in samples collected on days 0, 1, 2, 4, 6, 14, and 21 pi, at the University of Guelph Animal Health Lab (Guelph, Ontario).
Expression of these assays was quantified in samples from pancreas, pancreatic islets, colon, liver, monocytes, skeletal muscles, subcutaneous adipose tissue and lymphoblastoid cell lines.
Concerning our data on progranulin in spot urine, the adipokine was quantified in samples of 29 sex-matched patients of each chronic kidney disease stage (N = 145), which were randomly assigned using SPSS software version 18.0 (IBM, Armonk, NY).
The experiments were conducted using a murine secreted alkaline phosphatase (mSeAP), whose production can be quantified in blood samples as well as on tissue sections.
