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Plutonium in the fractions from the sequential extraction was separated by ion exchange chromatography and measured using alpha spectrometry.
Lutetium is separated by ion exchange.
The pigments were separated by ion pairing reverse phase HPLC, as described by [38] and modified by [39].
Total [H]IPs were separated by ion exchange chromatography and measured by liquid scintillation spectrometry.
In this technique, ions are first separated by ion mobility and then analyzed by TOF mass spectrometry.
Two enzymic activities in human liver homogenates were separated by ion exchange chromatography and the profile differed when activity was measured with p-AS and with sulphamethazine.
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Inorganic ions also can be separated by ion-exchange chromatography.
Metallothionein was extracted and separated by ion-exchange high performance liquid chromatography (HPLC), previous saturation with cadmium chloride.
Fractions of MBP alone obtained from the cleavage of MBP/exochitinase and separated by ion-exchange chromatography.
Analytes were separated by ion-pairing liquid chromatography using tetrabutylammonium ions and detected using UV absorption and fluorescence.
Lanes 5, 6, and 7. Fractions of pure exochitinase obtained from the cleavage of MBP/exochitinase and separated by ion-exchange chromatography.
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