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The LSB of each speech sample is inverted and obtained a modified speech signal.
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The thawed sample was inverted several times to ensure proper mixing and diluted 10-fold with filtered placebo buffer (PBS, pH 7.0 ± 0.2).
For confocal imaging, live samples were inverted and mounted on an inverted Olympus IX 81 microscope with confocal scanner unit (CSU-W1, Yokogawa, Japan) and imaged with a ×60/NA 1.42 oil U PLAN S APO objective.
The investigated samples are inverted high electron mobility transistor (HEMT) structures with embedded self-assembled InAs QDs which were grown in a molecular beam epitaxy (MBE) system.
After being incubated in the solution for 30 s and washed again with 1 × PBS, all samples were inverted onto coverslips, visualized, and photographed via a fluorescence microscope (Scope.A1, ZEISS) with a green filter.
It is necessary to note that the PV sign changes along the photon energy axis, and in Fig. 2, the spectra of both the samples are inverted by sign of voltage underneath 1.68 and 1.44 eV for the InAs/In0.15Ga0.85As and InAs/GaAs QD structures respectively.
Samples were inverted to avoid gradient effects, centrifuged briefly (2,000g, 5 minutes, 4°C) to remove any cellular elements, and aliquoted into polypropylene tubes for freezing and storage at −80°C [7].
Samples were inverted several times until a DNA mass formed.
The samples are inverted twenty times and left to sit at room temperature for 10 minutes.
Samples were inverted five times and incubated 24 h at 37 °C.
Samples were inverted three times and incubated at 37 °C for 2 h.
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