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After measuring the reference NMR spectra, the wild-type protein was treated with 5 mM H2O2 and spectra were recorded every 130 min.
The precision and accuracy of ICP-MS analyses were assessed by measuring the reference materials BE-N (basalt) and UB-N (serpentinite).
By measuring the reference Sx file, we found a value of approximately 69.6 Ohms.
Applying the reference design, as most studies do, results in the use of half of the gels for measuring the reference.
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Comparisons with the simulation results demonstrate that the multi-probe measurement method can also measure the reference bar mirror profile with a small standard deviation of 10 nm.
A light impact hammer and a laser vibrometer are used to measure the reference responses.
Two thermocouples to measure the reference and the sample temperatures were installed at each optimal position as DTA equipment.
When reference signals necessary for feedforward ANC configuration are difficult to obtain, the conventional ANC algorithms for multi-tonal noise do not measure the reference signals but generate them with the estimated frequencies [1].
Real-world evaluations lack measures of verification, are subject to biased sampling, rely on invalidated reports, do not explicitly define the reference goal or measure the reference goal inappropriately in terms of the method and are unable to distinguish between the effects of organisation, method and environment.
A modified strain-based failure assessment diagram (FAD) and a method of using the displacement of the outer boundary of the load (DOBL) to measure the reference strain in strain-based FAD (SB-FAD) application are established in this paper.
Once the maximum polarization was reached, a 30° rf pulse was applied and, after switching off the microwaves and waiting for a sufficiently long time for complete relaxation of the 13C nuclear spins, an identical 30° rf pulse was applied to measure the reference signal corresponding to the thermal equilibrium 13C polarization.
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