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The target analytes were extracted from the sample by two extractants, one of which is organic solvent placed inside the pores and lumen of hollow fiber and the other one is CNTs held in the pores of hollow fiber.
DNA was extracted from the sample using a commercial Nucleospin DNA extraction kit according to manufacturer's instructions with some modification (Clontech, CA, USA).
In both procedures, total lipids are first extracted from the sample, and then partitioned between a biphasic solvent system.
The extraction equilibrium was reached after 30 min, after which essentially the total amount (90 80%) of the four dinitrophenolic compounds were extracted from the sample.
Without tedious clean-up procedure, analytes were extracted from the sample to the adsorbent and organic solvent and then desorbed in acetonitrile prior to chromatographic analysis.
Analytes were extracted from the sample matrix with ethanol, and the extract, after dilution with water, was submitted to dispersive liquid liquid microextraction (DLLME).
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Chlorpyrifos were extracted from the samples by liquid-liquid extraction before the analysis.
PGE2 was extracted from the samples by solid phase extraction on a C18 cartridge.
Total RNA was extracted from the samples using Trizol (Invitrogen) extraction according to manufacturer's directions.
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).
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extracted from the template
recovered from the sample
extracted from the model
extracted from the testing
collected from the sample
extracted from the random
extracted from the prototype
generated from the sample
extracted from the instance
detected from the sample
calculated from the sample
extracted from the test
extracted from the lists
extracted from the specimens
extracted from the case study
extracted from the specimen
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