For ZnO photoanodes, tin-doped indium oxide (ITO) glass (Samsung Corning, 8.3 ohm sq−1, Korea) and PEN (Peccell, 13 ohm sq−1, Japan) were used as the substrates; 0.3 mM N719 dye anhydrous acetonitrile-tert butanol 1 1 solution was prepared for dye sensitization.
Cortactin (residues 1 336) or NtA (1 48) used in smTIRF were prepared for dye labeling by mutating all endogenous cysteines to serine and adding a KCK (Lys-Cys-Lys) tag at the C-terminus.
Table 6 Model validation for LPAC prepared for MG dye removal Activated carbon Model desirability Activation temperature, x 1 °CC) Activation time, x 2 (h) IR, x 3 MG dye removal LPAC yield Predicted Experimental Error Predicted Experimental Error LPAC 0.896 796 1.0 2.6 95.02 94.68 0.40 18.51 17.88 3.40.
Six sets of mesodiencephalic blocks were prepared for carbocyanine dye (DiI, Sigma, 468495) analysis.
A counter electrode was prepared for a dye-sensitized solar cell (DSSC) through electrochemical deposition of mesoporous platinum on fluorine-doped tin oxide glass in the presence of a structure-directing nonionic surfactant, octaethylene glycol monohexadecyl ether (C16EO8).
A flexible photoanode was prepared for a dye-sensitized solar cell (DSSC), using a titanium (Ti) foil as the substrate, titanium oxide nanotubes (TNTs) as the underlayer, and TiO2 nanoparticles (TNPs) as the overlayer; the TNTs were intended to provide one-dimensional (1-D) electron transfer paths at the interface of the Ti foil and the TNPs.
Polyvinyl alcohol (PVA) based gel polymer electrolytes (GPEs) with mixed iodide salts (KI and Bu4NI) have been prepared for application in dye sensitized solar cells and characterized using techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, and electrical impedance spectroscopy.
Three independent replicates were prepared for each strain and dye swaps were performed for each pairwise comparison making a total of six arrays for each of the three populations analysed.
Whole brains were collected into Bouin's fixative, embedded in paraffin and serial sections prepared for staining with cresyl violet dye.
Briefly, to preserve the heme signal, protein samples were prepared for SDS-PAGE with loading dye at 1 1 (v/v) that did not contain reducing agents, and the samples were not boiled.
Three primer set combinations (Loci 8, 4 and 7) were prepared for multiplex PCR with fluorescent dyes (Table 2) so that similar fragment sizes could be distinguished by different dyes.
