The regulation of that transcript was quantified by different complementary approaches.
Early experiments used labelled mycolactone, extracted from MU grown in C14 (Hong et al., 2008), but more recently, mycolactone concentration has been quantified by different methods.
These factors cannot be quantified by the same standard, and have different influences on different agricultural commodities in different wholesale markets, which brings great difficulty to the forecasting of agricultural commodity prices [1].
The relationship between the crown size and growing space requirements of different species can be quantified by equivalence coefficients that indicate, for example, how much growing space a beech may need on average in relation to a spruce of approximately the same tree diameter and stem volume.
The increased hazard of mortality for some PrP genotypes can be quantified by comparing the rate of mortality for different genotypes when defining mortality within periods as a binary trait.
As the rate of decrease in the comet parameters is attributed to cellular DNA repair, the efficiency of the cells to repair DNA strand breaks following different treatments can be quantified by determining the CRI.
Comprehensive investigation of the plasmid RMs was performed for their sequence, purity, homogeneity and stability, and then the concentration was quantified by three different methods: ultraviolet spectrophotometer (UV), high resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) and digital PCR.
Finally, subcellular phenomena are quantified by measuring different properties of the first and second channels, or by using additional organelle and molecule specific probes and extra fluorescence channels, for example in colocalization measurements [3].
CNAs levels in plasma from twenty-one acute P. vivax malaria patients from the Brazilian Amazon and 14 malaria non-exposed healthy donors were quantified by two different methodologies: amplification of the human telomerase reverse transcriptase (hTERT) genomic sequence by quantitative real time PCR (qPCR), and the fluorometric dsDNA quantification by Pico Green.
Apoptosis was quantified by four different methods.
