Sentence examples for analysis samples were treated from inspiring English sources

First of the analysis, samples were treated in a Universal 32R centrifuge (by Hettich Zentrifugen) at 4000 rpm, for half an hour at 4°C; successively they were filtered through disposable membranes Minisart, 0.2 μm in PTFE (by PBInternational).

We used the samples containing both extracellular and intracellular particles for the SEM analysis; samples were treated with 14% formamide solution and filtered onto a 0.8-μm carbon-coated Nuclepore filter (Millipore Filter Corp., Bedford, MA, USA).

For qRT-PCR analysis, RNA samples were treated with DNase I and purified with phenol/chloroform.

Before analysis, the samples were treated with trypsin to disperse the cells.

Prior to the TOC analysis, the samples were treated with 12.5% hydrogen chloride (HCl) solution to remove any inorganic carbon.

(b) In the case of LAB analysis, the samples were treated using spoilage lactic acid microflora isolated from the chicken meat.

For quantitative RT-PCR analysis, RNA samples were treated with DNAse I (Promega; 1 U/μg total RNA) for 30 minutes at 37°C according to the manufacturer's instructions.

For 7-OHC analysis, urine samples were treated with β-glucuronidase (250 U/mL; Sigma-Aldrich, Sydney, Australia) in 1.0 M acetate buffer (pH 5.0) at 37°C for 30 min. Concentrations of 7-OHC in the β-glucuronidase treated samples were quantified by the high-performance liquid chromatography system with C18-reverse phase column and a fluorescence detector (Walters et al. 1980).

To avoid DNA contamination that would disturb the quantitative mRNA analysis, the RNA samples were treated with DNase I (TaKaRa) following the instructions of the kit.

Before the analysis, all colostrum samples were treated as described earlier [ 14].

Before analysis, synovial fluid samples were treated with hyaluronidase (Hylase Dessau; Riemser Arzneimittel, Greifswald, Germany) at 37°C for 30 minutes and centrifuged at 3,500 rpm for 10 minutes.