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The 7-d mortality was 100% after a 24 h exposure to 7.5 g/m2 concentration of filter cake and 10 g/m2 of both powders.
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Within the nephron tubule the luminal CM concentration will increase from the filtered serum CM level to roughly 144 times that level as the tubules reabsorb salt and water (urine flow is 1000 mL/day or 0.69 mL/min; thus maximum concentration of filtered CM within the tubules is 100/0.69 or 144 times the serum CM concentration).
The concentrations of filter paper, corn steep liquor, cysteine hydrochloride and ferrous sulphate in the medium, which have been found to be optimal for ethanol production, were 45, 8.0, 0.25, and 0.01 g/l, respectively.
To examine the cytotoxicity of AuNPs in cancer cells, monocultures of the HeLa and MCF-7 cell lines were incubated for 24 h with increasing concentrations of filter (0.2 micron -sterilized AuNPs, and the cell viability was estimicron -sterilizedonversion AuNPs.
Required concentrations of filter -sterilized ANE (0.5 gL-1) or LPC (1.0 gL-1 equivalent of ANE) were added to molten (50°C) media, and plated in partitioned petri dishes (Fisher Scientific, Ottawa, ON).
Microarrays were washed manually with solutions containing decreasing concentrations of filter sterilized SSC 20× and SDS 10% (Sol.1: 1× SSC-0.2% SDS; Sol.2: 0.1× SSC-0.2% SDS; Sol.3: 0.1× SSC; Sol. 4: double deionized water).
Figure 11 Comparison of concentrations of filtered cadmium at WDP1 vs. predicted values based on solubility models from literature sources.
Figure 13 Comparison of concentrations of filtered arsenic at WDP1 vs. predicted values based on solubility models from literature sources.
For the following reactions: Figure 12 Comparison of concentrations of filtered iron at WDP1 vs. predicted values based on solubility models from literature sources.
Such a correlation is absent in the WDP1 data shown in Fig. 10. Figure 10 Comparison of concentrations of filtered copper at WDP1 vs. predicted values based on solubility models from literature sources.
Then, PHA production was induced by adding a 1.0%% (w/v) filter-sterilized glucose solution or different concentrations of filter-sterilized solutions of sodium glycolate [0.25, 0.50, 0.75, and 1.0%% (w/v)] and isopropyl β-D-1-thiogalactopyranoside (IPTG) (final concentration of 1 mM), and the bacteria were cultured at 30 °C for 72 h.
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