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Cell supernatants were collected for virus titration and soluble factor assays at the same times that RNA was harvested; the supernatant was frozen at −80°C until subsequent analysis.
Control F ab′ 2 antibodies were used in assays at the same concentration as the highest dose of TNT003.
The observed rate enhancements are similar to those seen in assays at the same glutathione concentration (2.4 mM) with thiosulfate as the sulfane sulfur donor.
Identical competitive fitness assays at the same ratio of competitors, but simply diluted by an extra 16-fold, demonstrated that the E2 population was actually more than three-fold more fit at this low initial density.
Figure 5 and 6 show antioxidant capacity of the six components identified from the extracts by using the DPPH and FRAP assays at the same concentration of 500 μM.
This assay allowed us to run many assays at the same time.
Similar(52)
Parallel cohorts were assayed at the same time under the same conditions and the experimenter was blinded to the genotypes or experimental conditions.
Standards (0.5, 1, 2, and 10 µM) of glutathione and a sample blank lacking glutathione were also assayed at the same time.
Unmanipulated HT1080 cells were assayed at the same time.
Concentrations of serum C-reactive protein (CRP) and plasma fibrinogen were assayed at the same time.
For each experiment, PBMCs from all individuals were thawed and assayed at the same time.
More suggestions(17)
determinations at the same
assignments at the same
analyses at the same
experiments at the same
papers at the same
concentrations at the same
measurements at the same
techniques at the same
tests at the same
replicates at the same
methodologies at the same
assays at the varied
assays at the central
assays at the non-cytotoxic
assays at the optimal
assays at the genomic
assays at the respective
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com