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Fluid samples were formulated up to 18 ppg density and passed contamination tests.
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In addition, when used in an affinity capture-buffer exchange format the final samples are formulated in a buffer compatible with most assays without requirement of additional downstream processing.
In the prediction system, a peptide sample was formulated by a 346-dimensional vector, formed by incorporating its physicochemical, sequence evolution, biochemical, and structural disorder information into the general form of pseudo amino acid composition.
To test whether adequate kinetic estimation could be obtained using IF corrected by fewer blood samples, three reduced sets of discrete blood sample data were formulated.
For tissue samples, the tissues were formulated into homogenates using saline solution.
Seven orange juices with equivalent sweet concentrations of different sweeteners (sucrose, sucralose, thaumatin, and four samples of stevia) were formulated.
Nine samples of vanilla milk desserts were formulated using a fractional factorial design.
First, experimental samples were analyzed and conclusions were formulated; and second, experimental sets were combined with publicly available microarray datasets and were further analyzed in search of common DE genes.
Based on the probe performance shown for histological samples, 8q24 and 3q26 probes were formulated into one probe set for testing and assessing their utility for cytology specimens.
To enable assessment of specificity and recovery two synthetic samples with known quantities of 174 synthetic miRNAs were formulated.
The questions were formulated in line with Experience Sampling Method principles to capture thoughts, feelings and behavior in real time.
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