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Results for the rate of absorption of carbon dioxide gas into a pneumatic (i.e. continuously rising) foam formed from a sodium carbonate bicarbonate buffer solution stabilised by a polyglycol frother are presented.
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The H+ ions are supplied by buffer solutions.
Buffered solutions were deoxygenated by vigorous sparging with nitrogen for at least 2 h.
An amount of 140 μl of a 10 mg/ml solution of lysosyme (Sigma-Aldrich, St . Louis MO, USA) in Tris-EDTA buffer (10 1 mM), pH 8, was added to each extraction tube and the samples were incubated at 37°C for 30 min. The DNA was eluted in 200 μl buffer AE (Qiagen) and stabilised by adding 4 μl of a 40 mg/ml bovine serum albumin (Ambion, Cambridgeshire, UK) and 2 μl of Ribonuclease-A.
In biological solutions, it is stabilised by forming complexes.
After HCl incubation, the sections were rinsed with Borate buffer solution followed by PBS rinses.
The results showed that the E0′ in Tris/cacodylic acid buffer solution shifted positively by about 10 mV in comparison with that in phosphate buffer solution.
The amplification was studied in phosphate buffer solution as electrolyte by determining the OECT transconductance.
Usually, the In-oxine solution is formulated in a buffer solution by the manufacturer.
Spectra were also obtained from the buffer solution (locations indicated by the blue circles), and no traceable SWCNT was found in the buffer solution after 24 hours.
After Bradford assay the histone solution was set to 1 µg/µl, stabilised by adding PAGE loading buffer to 1× and stored at −20°C.
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