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1“... common analytical method for DNA separation. In order to evaluate the polymer effect, different kinds...”
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2“...), pentapeptide-3 (PP3) and prezatide copper acetate (PCA). All the analytes could be separated at 200 nm within...”
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3“..., and separation voltage. In method validation, calibration plots were linear over the range 40.0 ~ 500.0 μM...”
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4“...), in whole blood (100 μL). Effects of parameters on the separation were investigated. The analytes were...”
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5“... and sweeping buffer, RP and DRP were well separated. The method was validated with a linear calibration curve...”
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6“... countries. The objective of this study is to establish an analytical method for monitoring the presence...”
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7“... monitoring in patients are needed. After synthesizing, IONPs were equilibrated with analytes for 20 min...”
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8“... the current and normalizing the polarity when 95% of current recovered, the separation of anionic analytes...”
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9“.... The electrokinetic injection was carried out, followed by a high voltage of −20 kV for separation. When analytes...”
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10“...碩士 === 高雄醫學大學 === 藥學研究所 === 99 === In this study, a capillary electrophoresis (CE) method combined...”
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11“...% methanol and 65 mM SDS was used as the sweeping buffer to separate the analytes at −15 kV. During method...”
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12“... and polyglutamylated forms（n=2-7）. These analytes have been separated within 7 min using glycine buffer. On the method...”
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