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Because the sample volume is replaced, repeated sampling is possible without compromising blood volume.
In both experiments (15%and48%8% ethanol fraction), the extracted protein concentrations in the sample were 3.0 g/L, which means 15 mg of extracted protein per sample because the sample volume was 5 mL.
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Because the sample volumes were significantly reduced (50 μL–200 μL) before GC/MS analysis, an additional silica column was used to remove any additional impurities in the neutral and the methylated phenol fractions.
The measurement of breakthrough volume is important in solid-phase extraction because breakthrough volume represents the sample volume that can be preconcentrated without loss of analyte during elution of the sample.
The sample volume is 40 μg.
The sample volume was 90 mL.
The sample volume injected was 10 μL.
Large scatters occur in composition measurements using wavelength-dispersive X-ray spectroscopy (WDS) when only a few precipitates are captured in the X-ray sampling volume, because the measured signal represents an averaged composition of the precipitate and the matrix phase in the sampling volume.
The sampled volume was not replaced.
However, because of the limited sample volume for such systems, the scattering is weak, especially if the neutron beam has to be severely collimated in order to resolve distances of interest (typically 10 to several 100 nm parallel to the surface of the sample).
PCBs were not detected in the bedroom, which was on the second floor of the home, but the limit of detection was elevated because of the small sample volume (see Table 1).
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