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Bound compounds were eluted with a gradient of 30 80% MeOH, 0.1% TFA in water at 4 ml/min, and eluted fractions were collected every 2 min (fraction T1-25).
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Hydrocarbons and other non-polar compounds were eluted with petroleum ether (boiling point, 60-80°C 60-80°C
Sorped compounds were eluted from swabs with methanol, dried and resuspended in enzyme assay buffer.
Compounds were eluted with 4 mL 80% methanol containing 5 mM ammonium bicarbonate pH 8.5.
The adsorbed organic compounds were eluted with MeOH.
Arsenic compounds were eluted with a phosphate buffer [ 44].
The resin was collected by filtration, and the compounds were eluted using acetone.
Compounds were eluted from the column with a gradient containing water and acetonitrile.
Retained compounds were eluted from the solid phase with 40% MeOH and analyzed on HPLC/UV.
After drying under nitrogen, the target compounds were eluted with 6 mL methylene chloride:hexane (1 1).
Using optimized chromatography conditions, the six compounds were eluted within 30 min in the sample analysis.
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