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We show that shearing the samples results in macroscopic alignment of both the micelle cubic crystal and the templated particles.
Lyophilizing the samples results in a reduction of backbone motion and reveals additional differences across the purification methods studied.
From such analyses, the Au film, in all the samples, results to be formed by spherical nanometric grains of increasing mean size [26].
One possible explanation for this discrepancy is incomplete receptor denaturation by SDS since boiling the samples results in aggregation.
No expression could be detected of COX-2 and TNF-α in any of the samples (results not shown).
The samples (results not shown) were again scattered about the verified global MLE of the quartet [ 5].
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Thermal treatment of the samples resulted in a shift of this peak to 1640 nm whereas it remained at the same position when the samples were digested with the proteinase K (Fig. 4, C, green and blue spectra, respectively).
All the samples resulted of sulfate geochemical type.
High optical quality of the samples resulted in low scattering level, and allowed us to neglect the scattering.
As shown, addition of proteinase K treatment to the samples resulted in partial loss of the band intensity.
For computational purpose, a value of 1∶5 was assigned to the samples resulting CF- or HAI-negative at 1∶10.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com