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Three basic classes of method exist for detecting FRET [17]. 1. Fluorescence lifetime imaging monitors the reduction in the fluorescent lifetime of the donor fluorophore that occurs upon energy transfer.
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Serial radiographic follow-up is advocated to monitor the reduction quality achieved at initial reduction.
Enzyme activity was determined by monitoring the reduction of NAD+ at 340 nm.
A convenient method for monitoring the reduction process is shown for a large number of precipitates simultaneously.
Electrochemical analyses were performed using cyclic voltammetry (IVIUM soft, Ivium Technology, Eindhoven, Netherlands) to monitor the reduction ability of the buffers.
This activity was measured spectrophotometrically at 25°C, by monitoring the reduction of acetyl-coenzyme A (acetyl-CoA) to CoA, at wavelength A 232.
Furthermore, the catalytic activity of these Ag NPs was investigated by monitoring the reduction of p-nitrophenol (4-NP) by NaBH4.
By periodically delivering the gas tracer and monitoring the reduction in concentration of the tracer from the permeable chamber, the groundwater velocity was determined multiple times daily.
The catalytic activity is investigated by monitoring the reduction of 4-nitrophenol by NaBH4 in presence of these silver nano-composite particles.
The method used by Roy and Barik (2010) was adopted in monitoring the reduction of Ag+ to Ag0 by measuring the absorption spectrum of each reaction mixture (silver nitrate solution + plant extracts) with a T-60 UV vis spectrophotometer.
Upon constructing this molecular architecture on a disposable gold electrode in a flow cell, amperometry was conducted to monitor the reduction current of benzoquinone produced from a catalytic reaction of horseradish peroxidase.
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