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The extracted collagen was further characterised by physicochemical techniques such as SDS-PAGE, circular dichroism and infrared spectroscopy.
A lysozyme specific homo-VHD was further characterised with an apparent affinity determined to be 216±6.6 nM.
hNET function in SupT1/FLuc.2A.RQR8.2A.hNET cells was further characterised via radiosubstrate uptake assay.
(b) hNET function in SupT1/hNET.2A.FLuc.2A.RQR8 cells was further characterised with an 125I-MIBG radiosubstrate uptake assay.
Thus, the electrical connection between the mechanically polished Cu nanowire arrays and the bottom Si substrate (for the sample in Figure 3d) was further characterised using a Dimension D3100 scanning probe microscope (Veeco, Plainview, NY, USA) in conductive atomic force microscopy mode (C-AFM).
SpARC1 localisation was further characterised in an independent expression system.
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After this initial characterisation, the strains were further characterised using molecular methods.
The samples were further characterised by nitrogen adsorption, NH3-TPD, XRD and scanning electron micrography techniques.
Selected antibodies were further characterised by kinetic analysis and a sandwich-based immunoassay developed.
The moisture content and mechanical properties of the developed porous scaffolds were further characterised.
The films were further characterised by X-ray photoelectron spectroscopy to establish their interfacial elemental composition.
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