Figure 4b shows that as pair-distance decreases between the core-shell cylinder pairs, the intensity of the plasmon mode, of approximately 1100 nm, decreases and is red-shifted.
Pearson's correlation coefficients were generated for background-subtracted image pairs using the Intensity Correlation Analysis plugin in ImageJ.
Similarly, solutions for the value of the susceptibility ratio ρ can be formed from ratios of the any pair of the intensity terms U, V, and W. While solutions of ρ should be independent of the calculation method, noise in the data present variations in the values extracted by each algorithm.
For the larger population of neuron pairs whose the minimal activation correlations were above a set threshold value of 0.05 3155 pairs for the intensity-invariant group and 254 pairs for intensity-modulated group), similar results were observed.
Cells knocked down for eEF1A1 showed half (pair A) or third (pair B) of the intensity of transcription per cell.
In region I, cross-peaks are observed among all four A T base pairs, but the intensities of the cross-peaks between the T8 A15 and T4 A19 base pairs are weaker then the NOEs between the T14 A9 and T20 A3 base pairs.
For each pixel, an ordered pair containing the intensities at that particular coordinate from both images was plotted.
However, compared with the FRB/N(1 437) – FKBP/C 394 547) pair, the signal intensity was lower, and the resultant S/B ratio was rather unstable, albeit not low (Additional file 1: Figure S1F).
For these three pairs of resonances, the intensity ratio of the shifted to unshifted peaks provides an estimate of the fraction of active to inactive enzyme complex.
The present results indicate that protein translation is tuned by codon (pair) usage, and the intensity of the regulation is associated with genome size, tRNA gene number, and G + C content.
