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Composites were prepared by mixing appropriate amounts of the two solutions inside 1.5 mL vials.
The microemulsions were prepared by mixing appropriate amounts of isooctane, AOT, and ethylene glycol.
Composites of P3HT and SWNTs were prepared by mixing appropriate amounts of the two materials dissolved in 1,2-dichlorobenzene.
Standard solutions were prepared by mixing appropriate amounts of the stock solution with ultra-pure water in 5 mL volumetric flasks.
The precursor solution was prepared by mixing appropriate amounts of titanium tetraisopropoxide, isopropyl alcohol, and Triton X-100 in an airtight vessel.
In one oligonucleotides one cytosine residue was replaced with 5-methylcytosine, allowing the exact adjustment of different methylation levels between 0% and 10% by mixing appropriate amounts of these well-defined oligonucleotides.
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Finally, emulsion PCR reactions were carried out by mixing appropriated amount of libraries with SOLiD beads.
Microemulsions were prepared by mixing weighed appropriate amounts of the individual components.
ATPS were prepared in 15-mL graduated tubes by mixing the appropriate amounts of PEG-4000, (NH4)2SO4, and enzyme solution.
Compound Gd ⋅1 was prepared in situ by mixing the appropriate amounts of ligand and GdCl3 ⋅6 H2O (99.99 %; Aldrich) in H2O followed by adjustment of the pH with NaOH aqueous solution (pH 7.4) for relaxivity measurements.
Cyt c was mixed with appropriate amounts of stock solutions of ligands to a final concentration of 0.5 μmol L−1 with different concentrations of ligands at 3, 4, 5, 6 and 7 μmol L−1, respectively, giving the molar concentration ratios of 1 6, 1 8, 1 10, 1 12 and 1 14.
More suggestions(15)
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