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在微制造毛细管阵列电泳装置上进行的高通量单链构象多态性分析。

High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device.

作者信息

Tian Huijun, Emrich Charles A, Scherer James R, Mathies Richard A, Andersen Paal Skytt, Larsen Lars Allan, Christiansen Michael

机构信息

Department of Chemistry, University of California-Berkeley, Berkeley, CA 94720, USA.

出版信息

Electrophoresis. 2005 May;26(9):1834-42. doi: 10.1002/elps.200410205.

Abstract

A high-density 384-lane microfabricated capillary array electrophoresis device is evaluated for high-throughput single-strand conformation polymorphism (SSCP) analysis. A delayed back bias direct electrokinetic injection scheme is used to provide better than 10-bp resolution with an 8.0-cm effective separation length. Separation of a HaeIII digest of PhiX174 yielded theoretical plate numbers of 4.0 x 10(6). Using 5% PDMA containing 10% glycerol and 15% urea, 21 single-nucleotide polymorphisms (SNPs) from HFE, MYL2, MYL3, and MYH7 genes associated with hereditary hemochromatosis (HHC) and hereditary hypertrophic cardiomyopathy (HCM) are discriminated at two running temperatures (25 degrees C and 40 degrees C), providing 100% sensitivity. The data in this study demonstrate that the 384-lane microCAE device provides the resolution and detection sensitivity required for SSCP analysis, showing its potential for ultrahigh-throughput mutation detection.

摘要

对一种高密度384通道微制造毛细管阵列电泳装置进行了评估,用于高通量单链构象多态性(SSCP)分析。采用延迟反向偏置直接电动进样方案,在有效分离长度为8.0厘米的情况下,可提供优于10碱基对的分辨率。PhiX174的HaeIII酶切产物的分离产生了4.0×10⁶的理论塔板数。使用含有10%甘油和15%尿素的5%聚二甲基丙烯酸酯,在两个运行温度(25℃和40℃)下区分了来自与遗传性血色素沉着症(HHC)和遗传性肥厚性心肌病(HCM)相关的HFE、MYL2、MYL3和MYH7基因的21个单核苷酸多态性(SNP),灵敏度达100%。本研究中的数据表明,384通道微CAE装置提供了SSCP分析所需的分辨率和检测灵敏度,显示了其在超高通量突变检测方面的潜力。

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