Alternatively, methods enabling direct estimation of halide concentration have been developed as e.g. the classic colorimetric mercury-iron-thiocyanate method (Cirello-[Egamino and Brindle 1995], Iwasaki et al., [1952], Zall et al., [1956]), iodide detection via starch incorporation (Kurtovic et al., [2007]) or quenching of fluorophores by halides ([Marchesi 2003]).
A quantitative analysis approach was developed, which corrects for the presence of air and blood in the lung (qABL method), enabling direct estimation of the metabolic rate of FDG in lung tissue.
Implemented method enables direct measuring of two invasion parameters (invasion area and number of invasion dots), automated calculation of three relative variables (invasion relative area, invasion dots relative density, and invasion dot average area), and the establishment of strain specific frequency histograms.
The previously proposed method enables direct image matching between protected images.
In contrast, our new method enables direct trafficking between the endothelial and tumour cells through secreting factors from each cell type.
This method enabled direct western blot comparisons of the expression of all four murine IgG receptors (FcγR) and complement receptors 3 (CD11b/CD18b/CD18) and 4 (CD11c/CD18c/CD18) on MGCs and M2 macrophages they derive from.
The method enables direct comparison between two experimental populations as well as measuring these two populations in relation to a third reference sample, allowing comparisons within the slide and across slides.
To summarize precursor intensities or spectral counts to protein intensities, the TopN (Ludwig et al., 2012; Malmström et al., 2009; Silva et al., 2006), iBAQ (Schwanhausser et al., 2011), APEX (Lu et al., 2007), NSAF (Zybailov et al., 2006) and SCAMPI (Gerster et al., 2014) methods are provided, enabling direct comparability of the quantitative results.
The "Vernalis generic compound set" [22] has been used in several studies to evaluate the performance of conformational sampling methods enabling a direct comparison of BCL Conf to other methods [23, 24].
The indirect assessment of airway inflammation, however, does have its limits and therefore there will always be a need for methods enabling a direct evaluation of airway inflammatory cell composition.
Both methods have the advantage of enabling direct calibration on one or more nodes of a phylogeny.
