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The cellulose columns (sodium form) had been equilibrated against 0.05 M sodium acetate buffer, pH 4.0.
mRNA stocks were diluted to 100 µg/ml in 25 mM nuclease-free sodium acetate buffer, pH 5.2 (NaOAc).
Better results for enzymatic hydrolysis were obtained when sodium acetate buffer was used.
Further, sodium acetate buffer was taken as a variable to optimize the polysaccharide additives.
Kinetic solubility studies were performed for the prepared solid dispersions, using sodium acetate buffer (pH 4.5).
Recombinant proteins at dilution 1 µg/ml in a corresponding buffer i.e. Peroxiredoxin 2 and CCDC101 in sodium acetate buffer 100 mM (pH 4.9).
Amperometric measurements were conducted at −0.7 V vs. Ag/AgCl in 50 mM sodium acetate buffer at pH 4.5.
Electrochemical behavior of the compound (1) was also studied by cyclic voltammetry (CV) in sodium acetate buffer solution.
0.25 M sodium acetate buffer (Panreac) at pH 4.75 was used as a supporting electrolyte.
These assays contained 50 mm sodium acetate buffer and 0.2 mm ABTS.
After incubation, sample was diluted 10 fold by adding 200 mM sodium acetate buffer (pH 5.0), followed by incubation with 1.5 mM pNP-Glc in 20 mM sodium acetate buffer (pH 5.0) at 37°C for 10 min.
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