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Issue 20, 2011
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One-PCR-tube approach for in situDNA isolation and detection

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Abstract

Traditional real-time polymerase chain reaction (PCR) requires a purified DNA sample for PCR amplification and detection. This requires PCR tests be conducted in clean laboratories, and limits its applications for field tests. This work developed a method that can carry out DNA purification, amplification and detection in a single PCR tube. The polypropylene PCR tube was first treated with chromic acid and peptide nucleic acids (PNA) as DNA-capturer were immobilized on the internal surface of the tube. Cauliflower mosaic virus 35S (CaMV-35S) promoter in the crude extract was hybridized with the PNA on the tube surface, and the inhibitors, interfering agents and irrelevant DNA in the crude extract were effectively removed by rinsing with buffer solutions. The tube that has captured the target DNA can be used for the following real-time PCR (RT-PCR). By using this approach, the detection of less than 2500 copies of 35S plasmids in a complex sample could be completed within 3 hours. Chocolate samples were tested for real sample analysis, and 35S plasmids in genetically modified chocolate samples have been successfully identified with this method in situ. The novel One-PCR-tube method is competitive for commercial kits with the same time and simpler operation procedure. This method may be widely used for identifying food that contains modified DNA and specific pathogens in the field.

Graphical abstract: One-PCR-tube approach for in situDNA isolation and detection

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Publication details

The article was received on 12 Feb 2011, accepted on 19 Jul 2011 and first published on 30 Aug 2011


Article type: Paper
DOI: 10.1039/C1AN15116A
Citation: Analyst, 2011,136, 4254-4259

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    One-PCR-tube approach for in situDNA isolation and detection

    X. Huang, L. Hou, X. Xu, H. Chen, H. Ji and S. Zhu, Analyst, 2011, 136, 4254
    DOI: 10.1039/C1AN15116A

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