An electrochemical biosensor for double-stranded Wnt7B gene detection based on enzymatic isothermal amplification
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文摘
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ssDNA produced from dsDNA target using nicking enzyme exploited and polymerase extension.

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A low DNA content could be detect due to the isothermal amplification process.

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Both the specific recognition of nicking enzyme and hairpin self-assembly triggered recycling ensured the high selectivity of this method.

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The proposed strategy could be extended to the detection of other DNA by simply exchanging the corresponding DNA sequence.

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