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The 5-mM NiCl2 solution, our positive control, showed a severe cytotoxicity, and no significant variations were found between the experiments (data not shown).
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Certainly, there is still some error between the experiment data and the calculation result from the modified porosity model.
In contrast to the experimental data in artificial sandstone cores, the modified model of porosity variation reduces the error from that between the experiment data and the formula of Biot's model, which considers only the compaction of matrix and fluid.
In addition, we describe the performance and operational experience of the detector during the experiment data collection between 2001 and 2010.
Good agreement between the theoretical calculations and the experiment data on electron transport in the molecular system has been obtained previously[21, 22].
In line with these findings we found that our animals from the atherosclerosis study showed higher levels of three Th1 cytokines (i.e. TNF, IL-12 and IFNγ) as compared to mice from the aneurysm study, while three Th2 cytokines (i.e. IL-4, IL-10 and IL-13) were not different between the two experiments (data not shown).
The comparison between the related experiment data and the prediction of the theoretical model in this paper are well matched, and the theoretical results' variation tendency agrees well with the experimental results, which validate our theoretical model.
The high-resolution instrumentation enables direct comparison between the experiments and data recorded during natural earthquakes.
Moreover, the different chimeric and mutated KLF6 proteins revealed that fluorescence intensity varied between constructs but not between experiments (data not shown).
We tested a number of genes, GAPDH, PSMB2, RPL32, and PPIB, evaluated previously as internal controls for lung cells [47], but none of these were useful due to large variations between cell lines and/or between experiments (data not shown).
We observed a variation of 1°C for the unmethylated blood DNA peak and 1.5°C for the in vitro methylated DNA peak (negative and positive controls, respectively) as a normal variation between different experiments (data obtained from the comparison among 20 30 experiments for each gene, data not shown).
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