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An electrochemical gene detection assay utilising T7 exonuclease activity on complementary probe-target oligonucleotide sequences

机译:利用T7核酸外切酶活性对互补探针-靶寡核苷酸序列进行电化学基因检测的方法

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This communication describes the synthesis of an electrochemically active oligonucleotide probe and its application in sensing complementary oligonucleotides sequences using a T7 exonuclease enzyme. Target oligonucleotides are detected by hybridisation with a ferrocene labelled probe oligonucleotide followed by addition of T7 exonuclease. The T7 enzyme is a double strand specific exonuclease that removes the terminal 5' nucleotide of the probe sequence. The 5' nucleotide is attached to a ferrocene label, which is subsequently detected at an electrode using differential pulse voltammetry. Time and temperature resolved measurements were performed and an associated study using dual labelled fluorophore-quencher labelled probes was performed to confirm the validity of the electrochemical assay. (C) 2004 Published by Elsevier B.V.
机译:该通信描述了电化学活性寡核苷酸探针的合成及其在使用T7核酸外切酶检测互补寡核苷酸序列中的应用。通过与二茂铁标记的探针寡核苷酸杂交,然后添加T7核酸外切酶来检测靶寡核苷酸。 T7酶是双链特异性核酸外切酶,可去除探针序列的末端5'核苷酸。 5'核苷酸附着在二茂铁标记上,随后使用差分脉冲伏安法在电极上检测到。进行时间和温度分辨的测量,并使用双重标记的荧光团-猝灭剂标记的探针进行了相关研究,以确认电化学测定的有效性。 (C)2004由Elsevier B.V.发布

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