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The quantitative determination of MO was performed by measuring its absorption with a UV vis spectrophotometer (PerkinElmer Lambda-35).
The reduced nicotinamide-adenine dinucleotide formed was determined by measuring its absorption at 340 nm against a blank preincubated and incubated as above, but to which water was added instead of acetaldehyde.
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Esophageal acid exposure was determined using standard pH monitoring, and duodenogastroesophageal reflux was measured by a spectrophotometric method (Bilitec) that identifies bilirubin in the refluxate by measuring its characteristic light absorption spectrum.
The dough was further evaluated by measuring its strength and water absorption.
Each isoform concentration was calculated after measuring its cadmium content by atomic absorption spectrometry with inductively coupled-plasma.
Further, its concentration was determined by measuring UV absorption; the amount of the purified fragment was 72 µg, which corresponded to 1.2×1014 molecules.
The concentration of IR700 was measured by its absorption to confirm the number of fluorophore molecules conjugated to each Panitumumab molecule.
The protein concentration was also determined by measuring the absorption at 280 nm with a UV Vis system.
DNA melting and reassociation can be monitored by measuring the absorption of ultraviolet (UV) light at a wavelength of 260 nanometres (billionths of a metre).
First, the bandgap was characterized by measuring the absorption spectrum of MoS2, as shown in Fig. 2b for 40 nm MoS2.
The concentration of ICG was calculated by measuring the absorption with the UV Vis system to confirm the number of fluorophore molecules conjugated with each antibody molecule.
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