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The trough was carefully cleaned with chloroform and ethanol and then filled with DI water or aqueous DA solution.
Before the film preparation, the trough was carefully cleaned with chloroform and then filled with DI water.
The slides were first cleaned with chloroform to remove oil.
The homogeniser was cleaned with chloroform, ethanol and 3× DEPC water (Promega) between each sample.
Silicon nitride chips were precut, cleaned with chloroform (3×), dried with nitrogen, immersed in a piranha solution (70/30, H2SO4/H2O2, caution: piranha is extremely corrosive and can explode) for 30 min, extensively rinsed in water, dried with nitrogen, and heated to 160 °C for 5 min. The amino-functionalization was performed with the "room temperature method" as described before.
Similar(55)
Protein lysates were cleaned with methanol chloroform precipitation.
RNA was cleaned with RNA Clean-up kit (Macherey-Nagel).
Clean with the grain.
Clean with the solution.
The total RNA was treated with Dnase I for 1 hour, then cleaned by phenol chloroform extraction, precipitated in cold 100% ethanol, and resuspended in DEPC-dH2O with 1 μl RNase Inhibitor (Roche).
Tester and Driver amplicons were pooled and cleaned twice with phenol-chloroform for subsequent enzymatic cleavage of J and JTA adaptors.
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