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Preparation of solAC HCO 3 − co-crystals: 50 m m sodium bicarbonate was prepared in a solution consisting of 0.1 m sodium acetate (pH 4.8), 0.2 m trisodium citrate, 16 % PEG 4000, and 10%% glycerol.
If the vesicles are prepared in a solution containing small peptides and short nucleic acids such as RNA, each of the vesicles will contain a different set of components, so each represents a microscopic experiment.
Optimal activity of ruthenium hydroxide as a catalyst for the hydrogenation of CO2 to formic acid is achieved over a γ-Al2O3 supported 2.0 wt% ruthenium catalyst, which is prepared in a solution of pH 12.8 with NH3·H2O as a titration solvent.
Liposomes are first prepared in a solution of sodium alginate.
Palmitate was prepared in a solution bound to fatty acid-free bovine serum albumin (BSA).
The dyes employed for TPEF excitation/emission measurements were prepared in a solution.
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Testing solutions were prepared in a solvent composed of saline 0.9% NaCl solution with 10% DMSO and 3% Tween 80.
The DPPH solution was prepared in a stock solution of 5 mL/2 mL in ethanol (EtOH) and wrapped with aluminium foil.
All solutions were prepared in a stock solution containing 3.4 m M trisodium citrate, 0.1% (v v−1) Nonidet P-40, 1.5 m M spermine, 0.5 m M tribase, pH 7.6.
Aqueous solutions of Cd (II) and Ni (II) ions for the batchwise experiments were prepared in a buffer solution (0.1 M HNO3 and 0.1 M HEPES [ N-[2-hydroxy ethyl] piperazine-N′-N-[ N-[2-hydroxynic acid])], pH 3.0.
The solutions of different concentrations of Bi III) ions ranging from 0.001 to 1 ppm were prepared in a buffer solution of pH 4.
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