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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device
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High-throughput single-strand conformation polymorphism analysis on a microfabricated capillary array electrophoresis device

机译:微型毛细管阵列电泳仪的高通量单链构象多态性分析

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摘要

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 φ X174 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° C and 40° C), providing 100% sensitivity. The data in this study demonstrate that the 384-lane μ CAE device provides the resolution and detection sensitivity required for SSCP analysis, showing its potential for ultrahigh-throughput mutation detection.
机译:评估了高密度384通道微加工毛细管阵列电泳设备,以进行高通量单链构象多态性(SSCP)分析。延迟背偏置直接电动注入方案用于提供优于10 bp的分辨率,有效分离长度为8.0 cm。分离出φX174的HaeIII消化物,得到的理论塔板数为4.0 x 10(6)。使用含有10%甘油和15%尿素的5%PDMA,在两次运行中可区分HFE,MYL2,MYL3和MYH7基因中与遗传性血色素沉着病(HHC)和遗传性肥厚型心肌病(HCM)相关的21个单核苷酸多态性(SNP)温度(25°C和40°C)时,可提供100%的灵敏度。这项研究中的数据表明,384通道μCAE设备可提供SSCP分析所需的分辨率和检测灵敏度,显示了其超高通量突变检测的潜力。

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