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The differences that occur are due to the reduced weight of repeated samples in the analytical model (Table 2).
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For this purpose, the two synthetic samples used in the analytical application of the sensor, of 20 and 50 mg/L Cu2+ were further used for the adsorption experiment.
For Methanocorpusculaceae and Methanosaetaceae, there was no standard reference available; therefore, quantification could only be considered between samples in the same analytical session.
Other serum samples (and quality control samples) in the same analytical batch as the samples with very high concentrations had low concentrations.
Authentic bovine DNA and porcine DNA were chosen as the spike for the positive sample controls in the analytical method to ensure the specificity and sensitivity of the PCR were adequately controlled using the specified analyte.
Urinary concentrations of the five other metabolites were generally lower than the LOD for the amount of sample used in the analytical measurements, so we do not discuss these further.
Samples were analyzed in the Analytical Chemistry Section Laboratory of the Michigan Department of Community Health.
Standards were run at the beginning and end of the analytical batch, and QC samples were interspersed in the analytical batch.
Whole goosander pineal glands and 10 mg of each pulverized bone, brain and fish samples were used in the analytical procedure.
Seventy-three percent of the eligible participants in the cohort had a cord blood sample that was included in the analytical sample.
The proposed method was successfully applied for the determination of ferrocene in gasoline samples, and the analytical results agreed fairly well with the results obtained by reference UV-Vis and FAAS methods.
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