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We have imaged in real time the migration of individual Os atoms and Os2 dimers on these surfaces.
We determined the apparent rate of migration of individual Os atoms on the two multidoped graphenic surfaces (average from observation of 10 single atoms).
Similar to the movement of isolated individual Os atoms, the distance traveled by each atom of the Os2 molecule increases linearly with irradiation time on both surfaces.
Figure 1d shows the dependence of the cumulative path length covered by two individual Os atoms (blue: B/Se surface; yellow: B/S surface) on irradiation time on the two surfaces.
The doping creates anchoring points for individual Os atoms, slowing down their migration so that it is commensurate with the time scale of image capture on an aberration-corrected transmission electron microscope.
We found that an individual Os atom required irradiation for 70 ± 9 s on the B/S surface before hopping to another site, whereas on the B/Se surface, only ca. 1.5 ± 0.3 s of irradiation was required.
Similar(52)
Estrogenic activity of -17-β estradiol (positive control), p,p′-dicofol, racemic o,p′-dicofol [-o,p′-dicofol] and the individual o,p′-dicofol enantiomers was measured via quantification of β-galactosidase.
Unless otherwise specified, all of the corresponding simulated O NMR spectra were obtained by simulation of each individual O site using SIMPSON and summation of these spectra, resulting in the final spectra.
To further assess the likelihood of HGT within VRA and VRB of the O-antigen locus, we constructed maximum-likelihood trees based on individual O-antigen genes and compared them with the genome-wide SNP tree.
The individual O and H NMR shifts are assigned to specific oxygen and proton environments, the DFT results allowing us to assign the three H NMR signals seen at room temperature to specific local environments.
To simplify the description of the individual O-mannosyl glycans in this review, we have designated the three subtypes cores M1, M2 and M3 (Yoshida-Moriguchi et al. 2013).
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