›› 2007, Vol. 38 ›› Issue (4): 442-445.doi:

• 论著 • 上一篇    下一篇

微量核酸样品的双重限制性荧光标记技术

马文丽1*; 孟伟1 ; 郑文岭2   

  1. 1南方医科大学基因工程研究所,广州 510515;2基因组中心,广州 510800
  • 收稿日期:2006-11-23 修回日期:2007-04-06 出版日期:2007-08-06
  • 通讯作者: 马文丽

Double Fluorescent Labeling Restriction Method for Microarray Applications

  1. 1Institute of Genetic Engineering, Southern Medical University, Guangzhou 510515,China; BR>2Southern China Genome Center, Guangzhou 510800,China
  • Received:2006-11-23 Revised:2007-04-06 Online:2007-08-06
  • Contact: MA Wen-li

关键词: 双重限制性荧光标记, 聚合酶链反应, DNA芯片

Abstract: Objective To study the double restriction fluorescent labeling (DRFL) method for fluorescent labeling of trace DNA samples and its effect in enhancing the pathogen detection sensitivity of microarray assays. Method SARS-CoV RNA samples were reversely transcribed and then further amplified with the restriction display (RD)-PCR and fluorescently labeled by conventional restriction labeling directly with Cy-universal primer and the novel double labeling with Cy-universal primer and Cy-dNTP. The labeled samples were applied to the microarray with the viral probes, processed and analyzed. Results Compared with the conventional method, DRFL labeling resulted in 3.5835 times higher fluorescent intensity of all the SARS probes on average, even though increased fluorescent intensities for different probes varied considerably. Conclusion Signal to noise ratio can be enhanced by the DRFL method which improves the sensitivity of microarray technology in trace pathogen detections.

Key words: Double restriction fluorescent labeling (DRFL), RD-PCR, DNA microarray

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