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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.
Samples were prepared in a solution of 10 mM NaH2PO4 and 50 μM Na2EDTA containing 0.1 M NaCl (pH 7.0).
Briefly, a working solution of 2% annexin V and 1 μg/mL propidium iodide (PI) was prepared in a solution of 1× annexin binding buffer.
Briefly, a working solution of 2 μM calcien AM and 4 μM ethidium homodimer-1 (EthD-1) was prepared in a solution of sterile 1× PBS.
The catalytic activity of the nanoparticles was investigated by measuring their ability to destroy a model fluorescent dye such as Rhodamine B. The samples were prepared in a solution of the model dye and nanopure water at 10 μM.
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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.
Prior to inoculation, the cells were prepared in a solution containing 1 1 mixture of PBS and Matrigel (BD Biosciences, San Jose, CA). 1 × 106 cells in 200 μl volume were injected subcutaneously in the right flank area of the mice.
The DPPH solution was prepared in a stock solution of 5 mL/2 mL in ethanol (EtOH) and wrapped with aluminium foil.
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.
Samples were prepared in a buffered solution of 10 mM NaH2PO4 (pH 7.0) and 50 μM Na2EDTA containing either 0.1 M NaCl or 1 M NaCl.
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