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A chromatographic method for determination of supercoiled plasmid DNA concentration in complex solutions

机译:色谱法测定复杂溶液中超螺旋质粒DNA的浓度

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A method for determination of the plasmid DNA concentration with subsequent analysis of the ratio supercoiled to open circular form is presented. The method is suitable for samples from all steps of the manufacturing process, from fermentation to final product. The analysis consists of size exclusion chromatography, followed by analytical thiophilic aromatic chromatography. in the first step, the plasmid DNA concentration is determined by group separation. including removal of RNA and other impurities, within less than 2 min. The limit of detection and quantification was 0.28 and 0.83 mu g/ml, respectively. The precision of the method is high, providing a coefficient of variation as low as below 2%. In the second step, the ratio of open circular to supercoiled plasmid DNA is determined following separation of the two plasmid DNA isoforms with a linear salt gradient. The precision of the second step was evaluated using serial injections of aliquots of a sample stock solution. In comparison with the two most commonly used methods, the developed analysis was found to be significantly more accurate than agarose gel electrophoresis and equivalent to capillary gel electrophoresis. The combined methods for quantification and control of homogeneity of plasmid DNA presented here enable reliable and precise analysis at all steps of the manufacturing process. (C) 2009 Elsevier B.V. All rights reserved.
机译:提出了一种确定质粒DNA浓度并随后分析超螺旋与开环形式比率的方法。该方法适用于从发酵到最终产品的所有制造过程样品。该分析包括尺寸排阻色谱,然后是分析性的亲硫芳香族色谱。在第一步中,通过组分离确定质粒DNA的浓度。包括在不到2分钟的时间内去除RNA和其他杂质。检测和定量的极限分别为0.28和0.83μg/ ml。该方法的精度很高,提供的变异系数低至2%以下。在第二步中,在用线性盐梯度分离两个质粒DNA同工型之后,确定圆形环状质粒与超螺旋质粒DNA的比例。使用样品储备溶液的等分试样的连续进样来评估第二步的精度。与两种最常用的方法相比,发现开发的分析比琼脂糖凝胶电泳准确得多,并且等效于毛细管凝胶电泳。本文介绍的用于定量和控制质粒DNA均质性的组合方法可以在制造过程的所有步骤中进行可靠而精确的分析。 (C)2009 Elsevier B.V.保留所有权利。

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