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The decrease in the ratio of the D/G bands may be explained in terms of an increase in the crystallite domains or a reduction in the quantity of amorphous carbon.
The identification of multiple bands may be explained due to the glycosylation heterogeneity in haptoglobin and partial cleavage of N-linked glycans by PNGase treatment.
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The absence of the 1680 cm−1 band may be explained by the non-use of separate polyisocyanate adducts as crosslinking agents, and therefore could be helpful to identify isocyanate free 1KWBPU systems.
Since the optical absorption also depends on short-range order in the amorphous states and defects associated with it, the decrease in optical band gap may be explained on the basis of "density of state model" proposed by Mott and Davis [34].
If one takes into account that oxygen atoms oscillate in such rings with more frequencies than in fourfold ones, such a band shift may be explained only by structural changes in the oxide network.
The reason for the double bands is unclear but may be explained by post-translational modification such as phosphorylation.
Discrepancies in the number of high molecular mass bands observed across different samples may be explained by the presence of isoforms specifically produced in pancreas [ 5] and differences in antibody antigen interactions between the two antibodies.
Insets are digital photographic images of A and B. Shifting of gold plasmon band to the higher value may be explained as follows: tomato extract is a strong reducing agent but not a good capping agent.
The high sensitivity of the three broad-band CBCL scales in our study may be explained by the use of face-to-face interviews to apply the CBCL to parents/caregivers (most of them low-educated), the application of the K-SADS-PL by an experienced child psychiatrist, and the rigorous methodological procedures adopted in our research.
The broadening and red shift of the plasmon band, as compared to the commonly reported region of 1100 1300 nm for Cu2– x Se and Cu2– x Se y S1– y NCs of various sizes and crystal structures, may be explained by considering such band as due to an "in-plane" resonance mode, analogous to that reported for CuS nanodisks.
It should be emphasised that the intensity of the Alq3 bands is not proportional to the amount of Alq3 in the samples, which may be explained by the different orientation of Alq3 in each sample.
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