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The cyclical reduction and oxidation reaction were performed in TGA equipment.
Isothermal and TPSR studies of deN2O reaction were performed over model MgO, and Co MgO systems.
Western blotting and reverse transcriptase polymerase chain reaction were performed to characterize the relative expression levels of desmocollin 2 isoforms.
Genomic and human papillomavirus deoxyribonucleic acid polymerase chain reaction and reverse transcriptase polymerase chain reaction were performed.
Starting from fully protected intermediate (5), appropriate modifications including Heck reaction were performed to furnish 3-O- 3-aryl-2-propenyl)leucomycin A7 analogues (9a–9m).
DNA assay, glycosaminoglycan (GAG) assay, hematoxylin eosin staining, Safranin-O staining and reverse transcription-polymerase chain reaction were performed to analyze the effect of the pore size on cell growth and the secretion of extracellular matrix (ECM).
Grafting reaction were performed according to Doehlert experimental design with temperature range fixed to 120 180 °C, time range 15 60 min and eugenol amount from 2 to 8 wt%.
A cell viability colorimetric assay, alkaline phosphatase assay and reverse transcription-polymerase chain reaction were performed to analyze the effect of pore size on cell growth, the secretion of extracellular matrix (ECM) and osteogenic differentiation.
Temperature-programmed reduction (TPR) and CO adsorption microcalorimetry along with the catalytic behaviour in the n-butane/H2 test reaction were performed in order to determine the specific interactions of Ru nanoparticles supported on different carbon materials.
In this study, three sets of photocatalytic reaction were performed using ΝΜ.
Reaction were performed in the presence glacial acetic acid as catalyst using microwave-assisted heating method.
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