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Cells were incubated with JC-1 (2 μM) for 15 min, and the ratio of green monomer (514-/529-nm excitation/emission maxima) to red J-aggregate (585-/590-nm excitation/emission maxima) was determined by flow cytometry using a FACSCanto cytometer equipped with BD FACSDiva software (Becton Dickinson, Heidelberg, Germany).
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For any of the remaining five ideal grid nodes a subset of local maxima is determined from the remaining local maxima in the scatter plot.
The F-P interferogram is a series of pulses, which are equally distanced in frequency/wavenumber domain, and the difference between adjacent maxima is determined by the free spectral range (FSR) of the interferometer.
Once the positions of these maxima are determined in the sampled clock data set, the corresponding samples in OCT data set can therefore be singled out, which are equal-spaced in the frequency domain with certain accuracy.
The full width at half maximum was determined using Fityk software.
The full width half maximum was determined for spread of excitation along the electrode array.
The magnitude of the maximum was determined by the contribution of gas phase pyrolysis products to filament growth.
The amount of sulfates is highest on average in areas of cavernous weathering, but the highest singular maximum was determined in the disintegrated area (4609 mg l−1).
Excitation maximum was determined for emission set at 516 nm.
One repetition maximum was determined according to procedures described by Kraemer and Fry.
The localization of this maximum was determined on the x- (medial-lateral), y- (anterior-posterior) and z- (inferior-superior) plane for the two measurements (pre- & post-training).
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