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Through the use of solid phase extraction (SPE), STX243 was extracted from the samples under vacuum using Oasis HLB Extraction Cartridges (Waters, Elstree, Herts, UK).
Chlorpyrifos were extracted from the samples by liquid-liquid extraction before the analysis.
Total RNA was extracted from the samples using Trizol (Invitrogen) extraction according to manufacturer's directions.
PGE2 was extracted from the samples by solid phase extraction on a C18 cartridge.
RNA was extracted from the samples using the RNeasy RNA extraction kit, as described above.
Lipids were extracted from the samples by a modified Bligh-Dyer extraction (Bligh and Dyer, 1959).
Analytes were extracted from the samples using conditioned C 18 solid phase extraction (SPE) cartridges (Waters Ltd., Watford, UK).
DNA was extracted from the samples, and tens of thousands of sequences of a specific bacterial gene were generated.
DNA was extracted from the samples and analyzed with a PCR-based identification assay.
DNA extracted from the samples was initially amplified with universal 16S ribosomal DNA primers.
The negative macroporosity was then extracted from the samples using a thermal process.
More suggestions(12)
generated from the samples
extracted from the prototypes
detected from the samples
removed from the samples
extracted from the swabs
extracted from the examples
collected from the samples
calculated from the samples
extracted from the lists
recovered from the samples
extracted from the testing
extractions from the samples
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