Sentence examples for determinations the samples from inspiring English sources

For these determinations, the samples were quantified from a single separation to increase the sample throughput.

For the Na+ and K+ determinations, the samples were completely digested in 12 mL 65% HNO3 and then analyzed on the ICP-OES spectrometer against National Institute of Standards and Technology traceable standards and controls.

For sIgA in colostrum and IgA in serum determinations, the samples were diluted at 1 5 (v/v) with saline solution (9 g/L), for IgM at 1 11 (v/v) and for IgG at 1 15 (v/v), and the antibody concentrations were determined using IgA (Bioclin®, Brazil, Ref K061), IgM (Bioclin®, Brazil, Ref K063) and IgG antiserum (Bioclin®, Brazil, Ref K062) diluted at 1 12 (v/v).

For enantio- and stereoselectivity determination, the samples were analyzed by supercritical fluid chromatography (see below).

For CODs determination the samples were first centrifuged at 10000 rpm for 30 minutes and then filtered (0.45  μm).

Prior to the metal determination, the samples were homogenized and then digested in organic matrices according to standard operating procedure (SOP) from ALS Group.

For the nonprotein thiol groups (NP) determination, the samples of S1 were precipitated with 200  μL of 10% trichloroacetic acid followed by centrifugation.

For titer determination, the samples from the three bleeds, as well as pre-immune serum, were tested for reactivity with the plant-derived PfGAP50-cTPH by enzyme-linked immunosorbent assay.

Inter- and intra-assay variations were calculated as the mean variation between ten individual determinations of eight QC samples (human serum) with each run consisting of two replicas of double determinations of the samples.

Before determination, the sample was diluted with 0.01 mol/l phosphate buffer pH 7.0 (Ransod, Randox, UK).

Prior to determination, the sample (~0.7 g) was degassed for 1.5 h at 110°C under vacuum (5 mmHg) to remove moisture and any other contaminants.