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The pH of the buffer was adjusted with orthophosphoric acid.
The pH* of the buffer was adjusted with diluted DCl or NaOD.
The pH* of the buffer was adjusted with diluted NaOD with a Solution Analyzer model 4603 instrument (Amber Science, Eugene, OR) equipped with a glass AgCl electrode (model 476086, Nova Analytics, Woburn, MA).
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The pH of the buffers was adjusted with diluted DCl or NaOD and measured with a Solution Analyzer Model 4603 (Amber Science, Eugene, Oregon) equipped with a glass/AgCl electrode (Model 476086, Nova Analytics, Woburn, MA).
The pH of the buffers was adjusted with KOH, and the final ionic strength of the motility buffer was 71 m m.
pH of the "cytoplasmic buffer" was adjusted to 7.4 with 1 M HCl and with 25 mM Pipes.
The pH of the buffer was adjusted to 7.3 with sodium hydroxide.
Next the buffer was adjusted to pH 6.0 with 20% HCl solution and filled up with ultrapure water to a total weight of 400 g.
The phosphate buffer was adjusted to pH 3.5 with 6 N HCl and partitioned three times into EtOAc.
The pH of the buffer was adjusted to 4.00 using 100 mM citrate buffer (pH 5.2) supplemented with 10 mM urea and the pH was adjusted to 7.00 using 10 mM phosphate buffer (pH 6.8).
In all assays, the incubation buffer was adjusted to 320 mOsm; when osmolarity could not be adjusted at this value; controls with the same osmolarity were used.
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