Exact(1)
Sampling was accomplished using a Conductivity, Temperature and Depth (CTD) probe Sea-Bird Electronicss, Bellevue, WA) and a rosette equipped with 10-liter Niskin bottles fitted with silicone closure springs.
Similar(59)
The Ar/O2 plasma oxidation processing of the samples was accomplished using a homemade plasma-enhanced CVD (PECVD) apparatus.
Sequencing of gland-derived samples was accomplished using traditional Sanger sequencing of individual clones.
Extraction of DNA from 134 plasma samples was accomplished using the High Pure PCR Template Preparation kit (Roche, Lewes, UK).
Calibration of dolomite samples was accomplished using a dolomite standard, whose isotopic composition was previously determined using classical offline preparation (provided by T. Vennemann, Lausanne).
Relative gene expression data (fold change) between samples was accomplished using the mathematical model described by Pfaffl (2001), using the mean ct score of 120 animals as the reference.
Isotope-dilution based quantIsotope-dilution basedntrations in tap water and blood samples was accomplished using solid--phase microextraction/gas chromatography (SPME/GC) with mass spectrometry (MS) (Cardinali et al. 2004) and high-resolution MS (Bonin et al. 2005), respectively.
Relative quantification of PS, PC, PE, and SM in each of control and phospholipid-incubated sample was accomplished using a calibration curve of phospholipid standards subjected to the same extraction procedure as the platelet samples; however, no platelets were present in the calibration solutions.
The band gap energies of pure and doped samples were accomplished using UV Vis-DRS analysis.
The potential applications of these magnetic solid phase extractors for removal of Ni II), Cd II) and Pb II) from drinking tap water, industrial wastewater and sea water samples were accomplished using a multi-stage micro-column technique.
TEM images of samples were accomplished using the following procedures: the cells exposed to Ag-ZnO/HNTs for 4 h were centrifuged and fixed with 2.5% glutaraldehyde overnight at 4 °C, followed by washing with 0.1 M PBS, and then postfixed with 1% osmium tetroxide for 1 h, dehydrated in graded concentrations of ethanol, and embedded in epoxy resin.
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