Xu Z Q, Hirokawa T, Nishine T, Arai A
Applied Chemistry, Department of Chemistry and Chemical Engineering, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyana, Higashi-Hiroshima 739-8527, Japan.
J Chromatogr A. 2003 Mar 21;990(1-2):53-61. doi: 10.1016/s0021-9673(03)00053-0.
The research adopted a single-channel microchip as the probe, and focused electrokinetic injection combined with transient isotachophoresis preconcentration technique on capillary electrophoresis microchip to improve the analytical sensitivity of DNA fragments. The channel length, channel width and channel depth of the used microchip were 40.5 mm, and 110 and 50 microm, respectively. The separation was detected by CCD (charge-coupled device) (effective length=25 mm, 260 nm). A 1/100 diluted sample (0.2 mg/l of each DNA fragment) of commercially available stepladder DNA sample could be baseline separated in 120 s with S/N=2-5. Compared with conventional chip gel electrophoresis, the proposed method is ideally suited to improve the sensitivity of DNA analysis by chip electrophoresis.
该研究采用单通道微芯片作为探针,并将毛细管电泳微芯片上的聚焦电动进样与瞬态等速电泳预富集技术相结合,以提高DNA片段的分析灵敏度。所用微芯片的通道长度、通道宽度和通道深度分别为40.5毫米、110微米和50微米。采用电荷耦合器件(CCD)进行检测(有效长度 = 25毫米,260纳米)。市售阶梯式DNA样品的1/100稀释样品(各DNA片段浓度为0.2毫克/升)可在120秒内实现基线分离,信噪比为2至5。与传统芯片凝胶电泳相比,该方法非常适合提高芯片电泳分析DNA的灵敏度。