Sun Kai, Li Zheyu, Ueno Kosei, Juodkazis Saulius, Noji Sumihare, Misawa Hiroaki
Research Institute for Electronic Science, Hokkaido University, Kita-21 Nishi-10, Sapporo, Japan.
Electrophoresis. 2007 May;28(10):1572-8. doi: 10.1002/elps.200600685.
We report the high fidelity, on-chip fractionation of selected segments from an electrophoretic flow of separated fragments. dsDNA fragments (10-330 base pairs (bp)) were initially separated using a 6.5 cm long channel with an electric field strength of 150 V/cm. As an example of the fractionation process, a target fragment of 20 bp was selected and extracted from the separation channel. The extraction was confirmed and evaluated by fluorescence imaging. High resolution and extraction fidelity were achieved by introducing new procedures for (i) extraction channel-blocking and (ii) segment transfer with cleaning. These procedures are necessary for the development of a practical, fully automated multitarget fractionation electrophoretic chip. A kind of CCD image processing method was introduced to monitor, control, and evaluate the procedure of fractionation. The resolution limits of the separation and extraction are discussed.
我们报道了从分离片段的电泳流中对选定片段进行高保真的片上分馏。双链DNA片段(10 - 330碱基对(bp))最初使用长度为6.5厘米、电场强度为150 V/cm的通道进行分离。作为分馏过程的一个例子,从分离通道中选择并提取了一个20 bp的目标片段。通过荧光成像对提取进行了确认和评估。通过引入用于(i)提取通道阻断和(ii)带清洗的片段转移的新程序,实现了高分辨率和提取保真度。这些程序对于开发实用的、全自动多目标分馏电泳芯片是必要的。引入了一种CCD图像处理方法来监测、控制和评估分馏过程。讨论了分离和提取的分辨率极限。