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Stable-isotope-labeled internal standards can help correct extraction loss, matrix effects, and instrument variability
Then, 40 mg of the product was purified by high-performance LC (HPLC) using the running mixture of iso-hexane/ethyl acetate (5:1) and obtained as a colourless solid (8.6 mg, 21%)
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Swim path was recorded using a computerized tracking system that displayed swim latency and swim distance [2]
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