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The solution was passed through a 100-μm filter.
The solution was passed through a 0.22-μm nylon membrane filter.
A sample of K5[BW12O40] (3 g) was dissolved in 60 ml water; then, the solution was passed through the resin column in the H+ form.
It is possible that the solution was passed through the columns at too fast a rate for complete binding of the anions.
After addition of H2O, the solution was passed through a 50 mm × 5 mm column containing a macroporous strongly acidic cation exchange resin, as previously described [1].
To separate the small molecule from the probe-DNA, the solution was passed through a NAP5 column using the DNA attachment buffer.
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Impurities, such as clay, sand, and oil, are removed by filtration, and the solution is passed through a stream of sulfur dioxide and then through a number of containers holding bundles of copper wire.
However, if the solution is passed through a new filter, no recovery was observed.
The resulting solution was passed through the column by a flow rate adjusted to the desired value.
The resulting solution was passed through the Sep-Pak tC18 Plus Long cartridge.
The lipid solution was passed through the extruder at least 19 times and diluted with PBS to 1 mg/mL.
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