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Through single nutrient lack experiment assay, necessary nutrient recipe for Acetobacter pasteurianus CICIM B7003 in acetous fermentation was confirmed.
For each experiment, assay, or morphological measurement, all selection and control lines were simultaneously evaluated.
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For the competitive inhibition experiment, assays were performed in duplicate in a final volume of 500 μl.
For lipid mixing experiment, assays were conducted in triplicate.
For leakage experiment, assays were conducted at least in duplicate.
This experiment assayed the effect of a small inner population on the growth of an outer population that was smaller than in experiment 1 (25 individuals).
Rather than considering the growth of a population, this experiment assayed the feeding rate of individuals, assessed as the number of vacuoles within an individual's cytoplasm.
Within each experiment, assays were set up in triplicate.
Real-time experiment assays confirmed that the proliferation rate was higher for HepG2 than HuH7 cells.
Upon investigation, we discovered the experiment assayed rhesus macaque tissue on a human genome-based microarray platform.
Since these enzymes had been previously purified and stored at −70 °C, the new experiment assayed them immediately after purification.
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