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利用缠结聚合物溶液和二极管阵列检测通过毛细管电泳进行多重DNA大小测定。

Multiplexed DNA sizing by capillary electrophoresis using entangled polymer solutions and diode array detection.

作者信息

Caruso Célia Sulzbacher, Lanças Fernando Mauro, Carrilho Emanuel

机构信息

Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos-SP, Brazil.

出版信息

Electrophoresis. 2003 Jan;24(1-2):78-85. doi: 10.1002/elps.200390034.

Abstract

We developed a method for the analysis of multiplexed double-stranded DNA (dsDNA) samples complexed to various intercalating dyes using entangled polymer solution. A commercial single-column capillary electrophoresis (CE) instrument with diode array detection was used for multiplexed detection of DNA samples by addition of intercalating fluorescent molecules. A Phi X174HinfI and a pGEM DNA ladder (1 mg/mL) were used for the electrophoretic separation of dsDNA fragments ranging in size from 24 to 726 and 36 to 2645 bp, respectively. The results suggested that simultaneous electrophoretic separation of different DNA ladders multiplexed with different dyes could be performed in the same capillary yielding fast DNA sizing separations. CE analysis, which is often overpowered by slab gel in sample throughput, could now overcome this disadvantage by allowing multiplexed sample analysis in a fraction of the time needed for slab gel analysis. The separation efficiency of stained DNA molecules with both dyes were dramatically improved with buffers containing a large cation such as tetrapentylammonium ion (Npe(4) (+)) as the only cation in the buffer.

摘要

我们开发了一种方法,用于分析与各种嵌入染料复合的多重双链DNA(dsDNA)样品,该方法使用缠结聚合物溶液。通过添加嵌入荧光分子,利用配有二极管阵列检测的商用单柱毛细管电泳(CE)仪器对DNA样品进行多重检测。分别使用Phi X174HinfI和pGEM DNA阶梯(1 mg/mL)对大小范围为24至726 bp和36至2645 bp的dsDNA片段进行电泳分离。结果表明,不同DNA阶梯与不同染料多重化后的同时电泳分离可在同一毛细管中进行,从而实现快速的DNA大小分离。CE分析在样品通量方面通常不如平板凝胶,但现在通过允许在平板凝胶分析所需时间的一小部分内进行多重样品分析,可克服这一缺点。当缓冲液中含有大阳离子(如四戊基铵离子(Npe(4) (+)))作为唯一阳离子时,两种染料对染色DNA分子的分离效率都有显著提高。

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