Sentence examples similar to ultrapure extracts from inspiring English sources

AE51 filters and the filters from the filterpacks sampled for 24 h were extracted with ultrapure water and then analyzed by Ion Chromatography (IC) to determine integrated SO42− concentration.

Ultrapure water and DNA extracted from known non-infected mouse were used as negative controls.

Negative controls included ultrapure water and DNA extracted from blood of a healthy person and a noninfected cat.

Tissues were homogenised with TRIzol® Reagent (Invitrogen) and a glass dounce homogeniser; total RNA was extracted using UltraPure™ (Phenol: Chloroform:Isoamyl Alcohol; Invitrogen), and then further purified using the RNeasy Kit (Qiagen).

For the determination of raffinose, stachyose and trehalose, 4 g of leaves and 1 g of roots were ground with liquid nitrogen and extracted with ultrapure water for 30 min at 80°C.

Pooled cartilage samples from all meniscectomized and nonoperated control LTPs were finely diced and extracted with 10 volumes of 4 mol/l GuCl and 50 mmol/l Tris HCl (pH 7.2) in the presence of proteinase inhibitors at 4°C with end over end stirring for 48 hours before dialysis of the extract against ultrapure water, as described previously [ 27].

6.4 g of the crude extract were suspended in 400 ml ultrapure water and the solution was extracted three times with 500 ml of solvents of different polarity starting with petroleum ether (PE), ethyl acetate (EA), n-butanol (BU) and finally water (ACE).

The degreased flowers were extracted twice by ultrapure water (W/V 1 12) that prepared with a Mill-Q water purification system (Merck Millipore Germany) at 85 ± 0.5 °C for 5 and 4 h.

Stock solutions were diluted in ultrapure water to make appropriate extract concentrations for testing.

The samples were extracted by 10 ml of ultrapure water with conductivity 0.08 μSm− 1 (Ultrapur, Watrex Ltd).

Denuders, Teflon filters and carbonate-coated backup filters were extracted in Milli-Q ultrapure water.