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Scaling of experimental data should be performed when comparing two datasets where a consistent difference can be detected between control probes designed to give equal signals at a range of different intensities.
Lower performance is found for serial signals which resemble components of a regular pattern in the two alternatives as, for example, reversed order (exp. 22: [Ø Y B Ø] vs [Ø B Y Ø]; exp. 36: [B B Y Ø] vs [Y B B Ø]; exp. 9: [Y B B Ø] vs [B Y B Ø]; exp. 38: [Y Y B Ø] vs [B B Y Ø]) or two equal signals in a series of three (exp. 33a: [Y Y B Ø] vs [Y B B Ø]).
Both media generated equal signals for IL-8.
With these settings, autofluorescent storage material yielded equal signals in cyan, yellow and red channels.
It is worth pointing out that the gradual decrease in unphosphorylated ERK1/2 was not caused by unequal loading, as the same samples loaded and probed for both GAPDH and unphosphorylated p38 showed almost equal signals over the time course.
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Here, we choose an equal signaling and sampling rate, i.e., M=1.
Complete tryptic digestion of a QconCAT protein produces equal molar peptide amounts, allowing verification of equal signal response of Hi3 peptides for the proteins of interest.
The measurement setup consists of two equal signal generation and data acquisition systems, as shown in Figure 1.
In particular, the performance for cell edge users, which have almost equal signal-to-noise ratios (SNRs) to several BSs, can be greatly improved since only the desired signals are amplified by the transmit precoding [31 33].
Therefore, under equal signal-to-noise conditions, we can expect a larger interval of variation of the interferometric phase around the ideal value for faster targets than for slower targets.
Equal signal intensities on both sides suggested that the transport property for Gd-DOTA of the blood-perilymph barriers on both ears did not change after transtympanic injection of LPNs (Fig. 2g, h) (Table 1).
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