Flow-assisted electrochemical corrosion of Cu Ni disc electrodes, subjected to a submerged impinging jet in saline water, was evaluated and quantified using the anodic current densities (ja), corrosion potentials (Ecorr), interfacial capacitances (C) and polarization resistances (Rp).
The hydrological response and sensitivity to climate warming of a snow-dominated watershed, the Upper Feather River Basin (UFRB) in Northern California, were evaluated and quantified using observed changes, detrending, and specified temperature-based sensitivity simulations.
On MRI, the coarctation and collateral vessels are evaluated and quantified using cine-SSFP or MR angiographic images (Fig. 5a).
Briefly, twenty nanograms of total RNA was isolated from lung tissue, cleaned, quality evaluated, and quantified using TRIzol (Invitrogen Corporation, Carlsbad, CA, USA), Qiagen RNeasy mini kit (Qiagen, Hilden, Germany) and Bioanalyzer (Agilent Technologies Inc., Santa Clara, CA, USA) respectively.
GFP expression for each condition was evaluated and quantified using a high content imaging system and software.
The presence of apoptosis was evaluated and quantified using flow cytometry in combination with Annexin V-fluorescein isothiocyanate (FITC).
Amplified cDNA Libraries were evaluated for quality and quantified using Agilent Bioanalyzer High sensitivity chip.
Expression of proliferating cell nuclear antigen, TGF-β, TGF-β receptors I and II, phospho-Smad2 and phospho-Smad4 was evaluated by immunohistochemistry and quantified using digital pathology.
Tumour protein marker expression will be evaluated on tissue microarrays (TMAs) and quantified using fluorescence IHC and the HistoRx® AQUAnalysis digital image analysis platform.
The quality of labelled cRNA was evaluated on the Agilent Bioanalyzer 2100 and quantified using a ND-1000 NanoDrop Spectrophotometer.
The quality of labeled cRNA was evaluated on the Agilent Bioanalyser 2100 and quantified using an ND-1000 NanoDrop spectrophotometer.
