Sentence examples for activity concentrations measured using from inspiring English sources

Real activity concentrations, measured using the available dose calibrator, are reported in Table 2. Absorbed dose calculations presented in the previous section were validated by absorbed dose to water measurements using LiF Mg,Cu,P chips inside a PMMA phantom filled with a homogenous 90YCl3 aqueous solution.

The activity concentration measured using the VOIs was evaluated using a concentration recovery coefficient (cRC), which was defined as: cRC=frac{left(frac{R_{mathrm{insert}}}{V_{mathrm{insert} }{widehat{S}}_{mathrm{vol}}}right)}{C_{mathrm{insert}}}, (1).

Luciferase activity was measured in extracts using the Luciferase Assay Reagent (Promega), according to the manufacturer's instructions, and values were expressed as relative light units normalized to the β-galactosidase activity or to the protein concentrations measured using the Bradford technique.

The blood activity concentration was measured using a gamma counter (WIZARD2, PerkinElmer LAS GmbH, Rodgau, Germany) cross-calibrated to the PET/MRI scanner.

The activity concentrations have been measured using a hyper-pure germanium detector.

Becker et al. proved that there is a strong linear correlation between apixaban plasma concentration and apixaban activity when measured using a standard laboratory chromogenic anti-Xa assay with either low molecular weight heparin or apixaban calibrators [ 43].

Thus, for all subsequent experiments, renal ACE2 activity was measured using a substrate concentration of 30 μM.

Labelled cRNA was purified with Qiagen RNAeasy Mini Kit and sample concentration and Cy3 specific activity were measured using a Nanodrop ND-1000 spectrophotometer.

Protein samples were diluted to the same concentration and β-galactosidase activity was measured using the substrate ONPG (O -nitrophenyl-β-D-galactopyranosidase, Singh Aldrich Co). as detcribed (Singh et al., 2009 ).

Protein samples were diluted to the same concentration, and β-galactosidase activity was measured using the substrate ONPG (O-nitrophenyl-β-D-galactopyranosidase; Sigma-Aldrich) as described by Singh et al.

SIRT1 activity levels were determined using recombinant SIRT1 (b; SIRT1 was incubated with AS101 or PBS at different concentrations for 1 hour. Activity was measured using the SIRT1 Fluorometric Activity Assay/Drug Discovery Kit Biomol (Exter, United Kingdom).