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On the movement and alignment of DNA during 120 degrees pulsed-field gel electrophoresis.

机译:关于120度脉冲场凝胶电泳中DNA的运动和排列。

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摘要

The displacement per pulse of lambda, T4, and G DNA during pulsed-field agarose gel electrophoresis has been measured for a fine mesh of pulse durations T between 0.02 and 120 s. The slopes of these curves show that the DNA moves by two distinct processes, designated 1 and 2, depending upon the pulse duration T. Process 1 operates at short T and causes dx/dT to decrease gradually with increasing T. This process is independent of molecular weight M. Process 2 is effective at longer T and causes dx/dT to rise sharply in sigmoidal fashion at a value of T which increases as M1.2, finally reaching a plateau of 1.4 microns/s for E = 4 V/cm. The shape of the dx/dT curve and its dependence on M lead directly to 4 zones of separation in plots of mobility vs M for different T. The alignment of the 3 DNAs during PFGE was measured by fluorescence-detected linear dichroism for E between 4 and 10 V/cm. These results are used in developing a molecular understanding of the mobility data.
机译:在脉冲场琼脂糖凝胶电泳期间,已测量了脉冲持续时间T在0.02至120 s之间的细网格,每个脉冲的lambda,T4和G DNA的位移。这些曲线的斜率表明,DNA根据脉冲持续时间T通过两个不同的过程移动,分别为1和2。过程1在较短的T上运行,并导致dx / dT随着T的增加而逐渐减小。方法2在更长的T时有效,并导致dx / dT以S形急剧增加,其T值随M1.2的增加而增加,最终在E = 4 V / cm时达到1.4微米/ s的平稳期。 dx / dT曲线的形状及其对M的依赖性直接导致了不同T的迁移率与M曲线中的4个分离区域。PFGE期间3个DNA的比对是通过荧光检测到的E在4之间的线性二色性测量和10 V / cm。这些结果用于发展对迁移率数据的分子理解。

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