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Plasma levels of lipid species, including ECs, were measured using liquid chromatography-mass spectrometry.
Also, apparent porosity and bulk density measured using liquid displacement method.
All Steep Hill samples were measured using liquid chromatography (LC), in Denver with Agilent LC equipment, in Seattle and Sacramento using Shimadzu LC equipment, and in Oakland using both types of machinery.
Vitamin D metabolites were measured using liquid chromatography-mass spectroscopy and PTH using a 2-site immunoassay from serum collected in 2000 2002.
BPA concentrations were measured using liquid chromatography-mass spectrometry in the maternal serum samples collected during 16-20 gestational weeks.
After initial incubation, OD595 was measured using liquid YE5S media as a blank.
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Urinary metabolites of a chlorinated OP, tris(1,3-dichloro-2-propyl) phosphate, and two non-chlorinated OPs, triphenyl phosphate and mono-isopropylphenyl diphenyl phosphate, were measured using liquid-chromatography tandem mass-spectrometry.
f_{{{text{ci}}_{text{g}}}} = phi_{text{ci}} cdot c_{i},.,p_{text{g}} ;quad i = 1,2, ldots n_{text{c}} (5) phi_{text{ci}} = fleft( {c_{i} cdot p_{text{g}} } right) (6 Afterword, the liquid second-phase fugacity (f li) is measured using liquid-phase pressure and the normalized second-phase liquid mole fractions (left( {x_{i}^{{prime }} } right)), as illustrated below.
Cells were then lysed in buffer containing 10 mM Tris, pH 7.4, 0.1% Triton X-100 and radioactivity measured using a liquid scintillation counter.
The change in adiabatic film cooling effectiveness on the downstream wall was measured using thermochromic liquid crystals.
Cells were lysed in 500 μl of 1% SDS for an hour and radioactivity was measured using a liquid scintillation counter (model Tri-Carb 2900TR; PerkinElmer Life and Analytical Sciences, Waltham, MA).
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