It would be important to develop further methods to measure protein quantities required to start the division cycle, in order to develop mechanistic models for bacterial growth phases.
If the proposed equivalence between partial molar entropy and absolute thermoelectric power is valid it opens the way for an experimental thermodynamic method to measure quantities that have previously been considered un-measurable, such as partial molar entropies of ions in solution and electric fields in homogeneous conductors placed in a temperature gradient.
We proposed an effective method to measure the quantity of Aβ peptides labeled with FITC using a p-FET with an on-chip single-layer optical filter.
As shown in Figure 1, we propose an effective method to measure the quantity of Aβ peptides labeled with fluorescein isothiocyanate [FITC] using a photosensitive field-effect transistor [p-FET] with an on-chip single-layer optical filter.
The experimental set-up consists of an original coupling of two techniques, a vibrating-wire sensor VW to weigh the polymer sample during the sorption and a pressure decay pVT-method to measure the quantity of gas, transferred from a high-pressure calibrated volume, which is absorbed by the polymer sample.
Furthermore, while this is a good method to measure the quantity of autophagosomes in a cell, it does not measure autophagic flux through the pathway and therefore suffers the same difficulties with interpretation that plague LC3 western blotting.
We used the Pfaffl analysis method to measure the relative quantity of gene expression (Pfaffl, 2001).
The ready availability of genomic and genetic information generated by high-throughput sequencing allows the application of advanced bioinformatic methods to characterize the quantity and distribution of the small and structural variants, and so clarify the effects of such genomic variants.
A standard normalization for miRNA expression analysis of serum samples using microarrays has not been established so far, but normalization of serum volume is reported to be the best method to determine quantity of miRNAs in blood using qPCR [ 67].
The forced molt was induced at 64 and finished at 67 weeks of age of all female WL-chickens by the method to reduce quantity and a calorie of the diet.
