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The model parameters specific to the particular membrane and mixture system are determined using liquid sorption and pervaporation experimental data.
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The mixture system was stirred for 30 min. Then, the transparent solution formed was separated into two parts.
Mixture design response surface methodology was used since the mixture system being studied has three or more components and one or more responses are analyzed and considered.
Prior to heating, the mixture system was cycled between vacuum and nitrogen three times, heated to 90°C and then was vacuumed for 10 min.
This result revealed that the suppression of CYP3A4 gene by the mixture system was specific and targeted CYP3A4 mRNA only, which further indicated that such shRNA mixture might become a powerful approach for studying CYP3A4 function.
The separation mechanisms of pure and mixture systems are identified through the analyses of simulation results.
In addition to the one-component polymer systems, simulation investigations of polymer mixture systems are discussed, both the polymer/polymer systems and polymer/nanoparticle systems are considered.
The pressure composition (P x) isotherms for the (CO2 + EGDMA) and (CO2 + DEGDMA) binary mixture systems were measured using the static method with a variable-volume view cell at temperatures ranging from (313.2 to 363.2) K.
The peptide lipid mixture systems composed of a combination of the lipid mixture of alkyl alcohol or soy lecithin to which peptides designed were added were desirable hysteresis curves similar to Surfacten® and amphiphilic Hel 13-5 peptide–lipids mixture systems were much more effective than the lipid mixture system.
XO inhibitory activity was expressed as the percentage inhibition of XO in the above assay mixture system and was calculated as follows: (4) % inhibition = (1 − Δ A / min test Δ A min blank ) × 100, where Δ A/mintest is the linear change in absorbance per minute of test material 10 and Δ Aminblank is the linear change in absorbance per minute of blank.
This is important because reaction products that may be entered into a chemical registration system are almost always mixtures unless extensive purification is done.
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