These solutions were neutralized with sodium hydroxide, filtered, aliquoted, and stored at −20 °C until use.
The slides were neutralized with 0.4 M Tris, pH 7.5 and stained with DAPI-Vectashield (Vector, UK).
Second, the resulting hybrid membranes were neutralized with triethylammine (TEA) and then impregnated with triethylammonium trifluoromethanesulfonate (TEATF).
The samples were neutralized with SDS, and DNA was digested with HindIII, dialysed, followed by immobilization to low surface coverage using streptavidin-coated magnetic beads19.
The carboxylic acid groups in the graft copolymers were neutralized with KOH, and films were prepared by solution casting.
To avoid unspecific adsorption of target DNA, any unreacted amino groups were neutralized with succinic anhydride according to standard hybridization procedures.
After centrifugation (14,000 g, 10 minutes, 4 °C), and supernatants were neutralized with a KOH solution, consisting of 3 M KOH, 0.3 M imidazole and 0.4 M KCl.
After this treatment the samples were neutralized with HCl.
The dried scaffolds were neutralized with 2 % NaOH and 4 % NaBr for 2 h and washed with distilled water.
The collected samples of acid and base hydrolysis were neutralized with sodium hydroxide and hydrochloric acid, respectively.
Then SWCNTs were neutralized with deionized (DI) water and trapped on a membrane filter (Millipore, 0.2 μm pore size, 47 mm diameter) using vacuum filtration.
