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Six samples with contrasting PSDs were assessed in duplicate.
Samples were assessed in duplicate.
Proximate composition, ferulic acid, total (TOTAX) and water-soluble (WEAX) arabinoxylans, were assessed, in duplicate, on native and fermented maize brans as previously reported (Manini et al. 2014).
Each sample was assessed in duplicate and every experiment was performed at least 3 times.
The amount of prostacyclin produced, calculated as the concentration of stable hydrolysis product, 6-keto-prostaglandin-F1α, was assessed in duplicate by a commercial EIA kit (Cayman Chemical).
Serum samples from days 0 and 21 post-vaccination were assessed, in duplicate, for their ability to neutralize an infection with ZEBOV-GFP in VeroE6 cells.
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The binding of antibody vectors to CA125 immobilized on the CM5 chip was assessed in duplicates across concentration ranges between 18.7 nM and 9.33 μM for MAb-B43.13 MAb-B43.13M and 19.6 μM for the scFv-B43.13, respectively.
All samples were assessed in duplicates.
Platinum concentration in cell suspension was assessed in duplicates by a GFAAS (graphite furnace atomic absorption spectrometry) system (Unicam M Series SOLAAR AA Spectrometer, Thermo Fisher Scientific GmbH, Dreieich, Germany).
We assessed in biological duplicate three of the reference time points in productive HCMV infection and mock infection (experiment "PM1", Figure 1A).
Samples were assessed in biological duplicate for each exposure condition primary pollutant exposures and time-matched unexposed controls, and PCA pollutant exposures and time-matched unexposed controls for a total of eight microarray samples.
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