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The cytotoxicity of different samples of carbon nanotubes synthesised by catalytic chemical vapour deposition was investigated towards human umbilical vein endothelial cells, using two cytotoxicity standard assays (neutral red assay for the cell viability and MTT assay tetrazolinium salt for the cell metabolic activity).
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The model reproduces the experimental hydrogen storage properties of different samples of activated carbons and carbide-derived carbons at 77 and 298 K and at pressures between 0 and 20 MPa, for an average nanopore width of about 5 Å.
In addition, the 1H NMR data on adsorbed water are shown to be consistent with the trends in the amount of pore volumes for different samples of activated carbons.
The X-ray scattering spectra of the different samples (electrolytes, dry carbon and impregnated carbons) are collected and corrected as detailed in the experimental section.
Samples of carbon nanofibers (CNF) with different carbon contents (6.5 55 wt.%) are prepared by decomposition of CH4 on Ni catalysts supported on silica glass fibers (SGF).
In this study four samples of carbon were obtained by thermal treatment at 1000 °C using as precursor the guava seed with different particle sizes.
It works with samples of carbon dioxide gas rather than solid carbon.
You will have different hormones, a different of carbon dioxide and so on.
Influence of the organic solvent on the yield of the extraction was first evaluated using two ash samples with different percentages of carbon.
For XRTS measurements, a narrow-bandwidth (ΔE/E<0.003) LCLS x-ray free electron laser (XFEL) beam at 5.07 keV was used to probe a dense carbon plasma produced in shock-compressed samples of different forms of carbon.
This method compares two samples that incorporate different isotopes of carbon or nitrogen (such as C, C, N or N), allowing the relative abundance of immunoprecipitated proteins to be determined in different samples, hence giving a quantitative measure of antibody specificity and affinity as described by Peach and colleagues.
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