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Fasting glycemia and total serum cholesterol were determined using a colorimetric enzyme immunoassay.
The concentration of uric acid was determined using a colorimetric enzyme assay on the Cobas Integra 400 plus analyzer.
The oxidase activity of Cp in serum was determined using a colorimetric enzyme assay where oxidation of p-phenylenediamine dihydrochloride was measured and thereby estimating the Cp concentration in mg/dl.
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Total serum cholesterol was measured using a colorimetric enzyme-based kit (Wako Diagnositics, Richmond, VA).
High-sensitivity C-reactive protein was measured using a colorimetric competitive enzyme-linked immunosorbent assay (CV 8.9%), as previously described (13).
High-sensitivity C-reactive protein (CRP) level was assessed at a median of 5.0 months from dialysis initiation, using a colorimetric competitive enzyme-linked immunosorbent assay (coefficient of variation, 8.9%).
NO and cGMP levels were measured using a colorimetric assay or enzyme immunoassay (EIA), respectively.
JNK phosphorylation was measured using a colorimetric fast-activated cell-based enzyme-linked immunosorbant assay (FACE ELISA) kit (Active Motif).
The reaction kinetics of alkaline phosphatase (ALP) adsorbed on paper was quantified by image analysis using a colorimetric technique under conditions of excess enzyme.
The activity of lysosomal enzymes was measured using a colorimetric assay (Froquet et al., 2008) and the kinetics of phagosomal proteolytic activity using the un-quenching of DQ Green BSA-tagged beads (Sattler et al., 2013).
The enzyme activity was measured using a colorimetric PAD activity assay modified from Knipp and Vasak.
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