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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Application of peptide nucleic acid to the direct detection of deoxyribonucleic acid amplified by polymerase chain reaction
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Application of peptide nucleic acid to the direct detection of deoxyribonucleic acid amplified by polymerase chain reaction

机译:肽核酸在直接检测聚合酶链反应扩增的脱氧核糖核酸中的应用

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摘要

Double-stranded DNA amplified by polymerase chain reaction (PCR) was detected by peptide nucleic acid (PNA) using a BIAcore super(TM) 2000 biosensor based on surface plasmon resonance (SPR). PNA is an artificial oligo amide that is capable of forming highly stable complexes with complementary oligonucleotides. We succeeded in the direct detection of double-stranded DNA, amplified by PCR with high-sequence specificity. It was shown that the target DNA was available for detection over the range of 40-160 nM. Therefore, the detection limit was 7.5 pmol of the target DNA (143 bases, applied volume 30 mu l). Our DNA detection system, the combination of BIAcore super(TM) and the probe PNA, could detect the target DNA with good reproducibility. In this report, we show that our system is a powerful tool for the diagnosis of pathologically significant DNA.
机译:使用基于表面等离振子共振(SPR)的BIAcore super TM 2000生物传感器,通过肽核酸(PNA)检测通过聚合酶链反应(PCR)扩增的双链DNA。 PNA是一种人工寡酰胺,能够与互补寡核苷酸形成高度稳定的复合物。我们成功地直接检测了双链DNA,并通过PCR进行了高特异性扩增。结果表明,目标DNA可用于40-160 nM的检测范围。因此,检测限为目标DNA 7.5 pmol(143个碱基,施加体积为30μl)。我们的DNA检测系统,结合了BIAcore super(TM)和探针PNA,可以以良好的重现性检测目标DNA。在这份报告中,我们显示了我们的系统是诊断具有病理学意义的DNA的强大工具。

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