The gypsum used in the experiments was extensively characterised using TGA, DSC, MIP, and NMR.
Moreover, the nanohybrid systems were extensively characterised, and the strong influence of pH on the formation of the semiconductor nanocrystals and their fluorescent response was verified.
Their occurrence has been most extensively characterised at the telomeric ends of eukaryotic chromosomes, whose DNA comprises such sequences, and where the extreme 3′ ends are single-stranded.
The nanobioconjugates were extensively characterised by several techniques, and the results demonstrated that the average size of ZnS nanocrystals and their fluorescent properties were influenced by the pH during the synthesis.
The recombinant thaumatins were extensively characterised using size exclusion chromatography for homogeneity, reversed-phase HPLC for purity (99%), peptide digest LC MS/MS for sequence determination, and circular dichroism and tryptophan fluorescence spectroscopies for conformational characterisation.
Foams of poly(lactide-co-glycolide) (PLGA) and poly(ɛ-caprolactone) (PCL) were extensively characterised using scanning electron microscopy, mercury porosimetry, dynamic mechanical analysis, degradation analysis, size exclusion chromatography and differential scanning calorimetry.
Batches manufactured at laboratory and pilot scales were extensively characterised, including an approach for the quantification of β-lactose in α-lactose based on powder X-ray diffraction (PXRD), which is described here.
The resulting mixtures were activated with a solution based on sodium hydroxide and sodium silicate, and their microstructure and mechanical behaviour were extensively characterised, using XRD, FTIR, SEM, BSEM/EDX and uniaxial compression strength (UCS) tests.
In this work, we will use data collected on a model paper collection to demonstrate the benefits of doing so: the SurveNIR historic reference paper collection [28] has been extensively characterised and pH and DP data for 665 real historic papers are used here.
β-catenin interactions with Lef1 and Tcf3 in the epidermis have been extensively characterised [4], [9].
It therefore seems probable that the absence of Gp210 from Fungi, where constituent Nups have been extensively characterised [48], is the result of secondary loss.
