The results were analysed via Analysis of Variance (ANOVA).
Interactions were analysed via western blottings using antibodies against specific endocytotic proteins.
The responses were analysed via descriptive analysis, grounded theory, and inferential statistics.
The sensitivity and reproducibility of the single-tube reagent were analysed via quantitative PCR assays.
To measure the difference in UV response quantitatively, both CN and KP were analysed via UV-vis spectrophotometry in reflectance mode.
Bulk and (1 0 0) surface vanadyl pyrophosphate, (VO 2P2O7, were analysed via periodic density functional theory calculations.
Total drug release and remaining content were analysed via UV-Vis and TGA, respectively, with both sets of results totalling the expected loaded amount for every stage of release (0 to 100%) within a ± 4% maximum margin of error.
The electric, optical and geometrical properties of the suspended tubes were analysed via the field dependence of the electric birefringence over a wide range.
Metabolic activity and DNA synthesis were analysed via MTS metabolic assay and [3H]-thymidine uptake, while ECM protein expression was determined by immunohistochemistry. TissuFleece®, Alloderm® and PLGA PCL mesh supported cell attachment, proliferation and neo-tissue formation.
Transcripts were analysed via memo-writing and diagramming techniques.
In order to verify FSS effects, cells were analysed via light and fluorescence microscopy.
