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For all tested samples, the quantity of ICG released and the unencapsulated ICG equaled the quantity of the ICG precursor, indicating that the mass balance was conserved.
For many applications, including metagenomics and the sequencing of ancient, forensic, and clinical samples, the quantity of input DNA can be critically limiting.
Nineteen samples were successfully radiocarbon-dated, while for three samples, the quantity of collagen in the enamel was not sufficient for this technique (Table 1).
Plasminogen activator inhibitor-1 and GAPDH mRNA variability were determined from triplicate samples, the quantity of which was in error by less than 10%.
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Given our interest in the changes in the expression of genes between samples, the quantities were finally converted to a logarithmic scale using a log base 2 conversion.
By changing the displacement pressure gradient of oil flow to drive the core sample, the quantity of the oil flow is measured at 158 °K.
For each sample, the quantity of the specific miRNAs and the reference genes was determined from respective standard curves.
For each sample, the quantity of telomere repeats and the quantity of 36B4 copies were determined in comparison to the reference sample.
For each sample, the quantity of specific hepatic marker mRNA was expressed as n-fold the normalized amount of mRNA from undifferentiated control cells.
For each sample, the quantity of specific hepatic marker mRNA was expressed as n-fold the normalized amount of mRNA from undifferentiated cells.
For each sample, the quantity of PEDV RNA GE was ≈10 times higher than plaque assay results for a cell-adapted PEDV strain, PC22A.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com