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However, although the biphasic shape of the curve was a constant feature, the relative maximum value of both peaks were different when ERα recruitment was compared between HeLa and MCF-7 cell lines, suggesting a role for cell specificity in the process.
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Obviously, under the same conditions, the red shifts for three peaks were different.
The intensities of the main peaks were different according to the growth angles.
The relative intensities of the PCDS peaks were different than those observed with conventional IR spectrum or FTIR method.
Although the peak potentials were in very good agreement with each other, but heights of the peaks were different for each electrode.
Moreover, the expression curve and the timing of the peaks were different for the wild type and mutant under SD conditions.
The signal intensities of these "twin" peaks were different from preparation to preparation, ranging from not detectable till up to three times higher than the non-modified form.
We also asked whether the species conservation of sequences and the AT or GC content in the 610 bp centered on the hybridization peaks were different from 610 bp sequences surrounding random potential SOX9 binding sites outside the peaks.
More specifically, we were interested in whether these peaks were different from the left vOT peak at y = −64 identified for all spelling conditions relative to the control conditions.
In our study, the H2AM isoform was present in both peaks and the composition of isoforms in the two peaks was different.
Also, the position of these satellite peaks is different in these two oxidation states.
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CEO of Professional Science Editing for Scientists @ prosciediting.com