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In the RDB-PAS measurement, electrons in the valence band of a powder sample are directly excited to electron traps (ETs) and accumulated in the ETs from the deeper (anodic) side to the shallower (cathodic) side by wavelength-scanned continuous light, and the increase in photoabsorption of electron-filled ETs is measured by modulated light at a fixed wavelength by PAS.
Using primers that can hybridize with these conserved portions, 16S rDNA sequences of most of the microbes (both culturable and un-culturable) in a given environmental sample are directly amplified, cloned and sequenced.
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The derivatized sample was directly injected into the HPLC system.
The sample was directly infused at 5 μL/min.
In addition, the coupling current time constant of the sample was directly measured.
The as-prepared sample was directly transferred to FESEM chamber for examination.
In this research, the actual image of the sample were directly considered in the FE.
After 24 h of immersion, the sample was directly annealed at 150°C for 1 min.
Following this incubation period, the sample was directly injected into a q-TOF mass spectrometer.
A commercially available catalyst sample is directly slurry-coated inside the microchannels.
In the second method, the sample was directly placed inside a freezer for casting at temperature of -40 ̊C.
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