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Blank extractions were included every five samples to monitor for contamination.
During the rotation process, the region's environmental agency took samples to monitor water quality.
Quality control (QC) samples for livers and sera were prepared from pooled partial study samples and injected every five study samples to monitor intra-batch precision.
A random sample of 438 participants returned for annual collection of blood samples to monitor adherence and safety (hypercalcemia), including repeat physical measurements at 12 months follow-up.
We also performed flow cytometry and viability analysis on samples to monitor changes in cell phenotype and apoptosis/necrosis that occurred during sample handling.
By using a chip-based platform that combines microfiltration and bioorthogonal nanoparticle targeting, we demonstrate for the first time that magnetic biosensing can be applied for clinical evaluation of circulating microvesicles in blood samples to monitor cancer therapy.
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Surrogate standards were added to each sample to monitor the extraction performance and matrix effects.
Surrogate standards were added to each sample to monitor extraction performance and matrix effects.
Instead of monitoring the temperature of the bath, a thermocouple was positioned inside the sample to monitor the temperature on the spot.
The first is a regular quality control sample to monitor the LC-MS response in time.
Second, blood sample collection is less invasive and safer, allowing for a larger sample size and repeated sampling to monitor disease progression.
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