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The object data were divided into 160 blocks, and a separate hologram was prepared for each.
After adding quantitative reagent of urea and creatinine, 1000 ml fresh blood of pig was prepared for each trial.
An integrated somatic and germ-line clinical report was prepared for each patient and officially signed out by a medical geneticist before being placed in the medical record.
A saturation mutagenesis library was prepared for each residue (Tyr110 and Asp111), and activity of the resulting variants was assayed on different chain length substrates.
A fresh ABTS solution was prepared for each assay.
A specific questionnaire was prepared for each data collection phase according to the child's age group.
A concentration of 10,000 nematodes/ml was prepared for each nematode.
A 1000 mL bulk sample was prepared for each sample type from one specific sampling site.
A calibration curve, at an appropriate wavelength, was prepared for each substance to help identifying the concentrations.
YMMM containing single phenolic substrates was prepared for each phenolic compound using the concentrations reported under "Results".
A blank was prepared for each measurement by replacing α-glucosidase with 10 mM potassium phosphate buffer.
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CEO of Professional Science Editing for Scientists @ prosciediting.com