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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >The effect of pore size in an ultrasensitive DNA sandwich-hybridization assay for the Escherichia coli O157:H7 gene based on the use of a nanoporous alumina membrane
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The effect of pore size in an ultrasensitive DNA sandwich-hybridization assay for the Escherichia coli O157:H7 gene based on the use of a nanoporous alumina membrane

机译:基于使用纳米多孔氧化铝膜的大肠杆菌O157:H7基因的超敏性DNA夹心杂交测定中的孔径在超敏性DNA夹层杂交测定中的影响

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摘要

The authors describe a rapid method for the detection of the Escherichia coli O157:H7 (E. coli O157:H7) bacterial gene. The DNA sandwich-hybridization impedimetric assay is based on the use of a nanoporous alumina membrane in combination with gold/silver core/shell nanoparticles (Ag@AuNPs) that act as tags for impedance signal amplification. The probe oligonucleotides were immobilized on the walls of the nanopores. This is followed by hybridization, first with target (analyte), then with reporter oligonucleotides labeled with Ag@AuNP tags. The impedimetric signal results from target oligo hybridization with probe oligos and cohybridization with labeled reporter oligos, which increases the blocking degree of the nanopores. The assays were tested with membranes in nanopore sizes of 20 nm, 50 nm and 100 nm. The assay performs best in case of 100 nm nanopores where the limit of detection is as low as 11 pM, with a linear detection range that extends from 50 pM to 200 nM. This indicates its potential for rapid and ultrasensitive gene detection.
机译:作者描述了检测大肠杆菌O157:H7(大肠杆菌O157:H7)细菌基因的快速方法。 DNA夹层杂交阻抗测定法基于纳米多孔氧化铝膜与金/银核心/壳纳米颗粒(AG @ AUNP)组合的用途,其起到阻抗信号放大的标签。将探针寡核苷酸固定在纳米孔的壁上。随后是杂交,首先用靶标(分析物),然后用记者寡核苷酸标记为AG @ AUNP标签。阻碍信号由靶寡核苷酸与探针寡核苷酸杂交产生,与标记的报告寡核苷酸的循环化,这增加了纳米孔的阻塞度。用纳米孔尺寸为20nm,50nm和100nm的膜中测试测定。该测定在100nm纳米孔的情况下表现最佳,其中检测限低至11μm,线性检测范围从50pm至200nm延伸。这表明它具有快速和超细基因检测的可能性。

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