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High-resolution liquid chromatography of DNA fragments on non-porous poly(styrene-divinylbenzene) particles.

机译:非多孔聚(苯乙烯-二乙烯基苯)颗粒上DNA片段的高分辨率液相色谱

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摘要

DNA restriction fragments and PCR products were separated by means of ion-pair reversed-phase high-performance liquid chromatography on alkylated non-porous poly(styrene-divinylbenzene) particles with a mean diameter of 2.1 microns. Optimum resolution was obtained by using an acetonitrile gradient in 100 mM of triethylammonium acetate and a column temperature of 50 degrees C. This allowed the separation of DNA fragments differing in chain length by 1-5% up to a size of 500 base pairs. PCR products could be analyzed directly in less than two minutes with a concentration sensitivity of at least 300 ng/ml. Compared with anion-exchange chromatography or gel electrophoresis no desaltation of the purified DNA molecules is required because the volatile buffer system can be readily evaporated. Subsequently, the method was used for the semiquantitative evaluation of the expression of multidrug resistance genes in mononuclear white blood cells.
机译:通过离子对反相高效液相色谱在平均直径为2.1微米的烷基化无孔聚(苯乙烯-二乙烯基苯)颗粒上分离DNA限制片段和PCR产物。通过在100 mM乙酸三乙铵中使用乙腈梯度和50°C的柱温获得最佳分离度。这允许分离链长相差1-5%的DNA片段,最大大小为500个碱基对。 PCR产物可以在不到两分钟的时间内直接进行分析,其浓度灵敏度至少为300 ng / ml。与阴离子交换色谱法或凝胶电泳相比,纯化的DNA分子无需脱盐,因为挥发性缓冲液体系易于蒸发。随后,该方法用于单核白细胞中多药耐药基因表达的半定量评估。

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