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The amount of buffer was adjusted for the amount of CdCl2 in 0.02 M HCl added (final pH 5.5).
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In order to provide identical amounts of DNA eluate the amount of elution buffer was adjusted to 100 μl for all kits.
The pH of the GPS buffer was adjusted to pH 7.0 and pH 9.0 for some experiments.
The pH of the EZ-TN reaction buffer was adjusted to pH 7.0 or pH 9.0 for some experiments.
If additional reagents, e.g. effectors or blocking DNA, were added, the amount of reaction buffer was adjusted accordingly and the assay was incubated for 10 min at room temperature before addition of labelled DNA.
The pH of the buffer was adjusted with orthophosphoric acid.
The pH of the buffer was adjusted to 7.4.
The pH of the buffer was adjusted to 7.4 using a precalibrated pH meter.
The pHs of these buffer was adjusted to 5 and 6, respectively.
Buffer was adjusted to desired pH using HCl and NaOH.
The pH of the elution buffer was adjusted to 3.9 using 0.3 M acetic acid.
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