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Whereas the 1695 cm−1 and 1624 cm−1 components can be definitely assigned to the intermolecular β-sheet interaction of the protein aggregates [21], [27], [28], the two other bands were assigned by other authors to different vibrational modes.
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Phylogenetic affiliations for each sequenced DNA band were assigned by comparison to known bacterial sequences recorded in the National Center for Biotechnology Information database [GenBank, [47]].
DNA fragments from the bands were sequenced and each OTU sequence and each sequence from the DGGE bands were assigned to taxonomic groups by BLAST using the GenBank nucleotide database as described above.
The observed NR bands were assigned to Raman-active CC stretching vibrational modes by comparison with calculations based on density functional theory.
Bands were assigned as upper, intermediate, and lower on the basis of density, as determined by refractometry at 25°C [ 31].
The CO absorption bands of the mixtures were assigned by using several infra-red techniques such as spectrum addition, spectrum subtraction and second derivative spectroscopy.
PFGE types were assigned by matching the banding patterns of isolates to those of the CHEF lambda DNA standard (Bio-Rad, 1703635) and to control strains of known USA type.
This diffusion of CO2 is indicated by the growth of IR bands being assigned to the stretching vibration of C O.
The absorption bands are assigned to π → π∗ transitions.
All bands are assigned to Thy.
All bands are assigned to Thy; the bands assigned to graphene oxide are noted.
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