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Rapid and quantitative measuring of telomerase activity using an electrochemiluminescent sensor

机译:使用电化学传感器快速和定量测量端粒酶活性的测量

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Telomerase, a ribonucleoprotein enzyme that adds telomeric repeats to the 3'end of chromosomal DNA for maintaining chromosomal integrity and stability. This strong association of telomerase activity with tumors establishing it is the most widespread cancer marker. A number of assays based on the polymerase chain reaction (PCR) have been developed for the evaluation of telomerase activity. However, those methods require gel electrophoresis and some staining procedures. We developed an electrochemiluminescent (ECL) sensor for the measuring of telomerase activity to overcome these problems such as troublesome post-PCR procedures and semi-quantitative assessment in the conventional method. In this assay 5'-biotinylated telomerase synthesis (TS) primer serve as the substrate for the extension of telomeric repeats under telomerase. The extension products were amplified with this TS primer and a tris-(2'2'-bipyridyl) ruthenium (TBR)-labeled reversed primer. The amplified products was separated and enriched in the surface of electrode by streptavidin-coated magnetic beads, and detected by measuring the ECL signals of the TBR labeled. Measuring telomerase activity use the sensor is easy, sensitive, rapid, and applicable to quantitative analysis, should be clinically useful for the detection and monitoring of telomerase activity.
机译:端粒酶,一种将端粒重复添加到染色体DNA的3'末端以保持染色体完整性和稳定性的核糖核蛋白酶。这种强烈的端粒酶活性与肿瘤建立它是最普遍的癌症标志物。已经开发了基于聚合酶链反应(PCR)的多种测定以评估端粒酶活性。然而,这些方法需要凝胶电泳和一些染色程序。我们开发了一种用于测量端粒酶活性的电化学发光(ECL)传感器,以克服常规方法中的麻烦后PCR程序和半定量评估等问题。在该测定中,5'-生物素化的端粒酶合成(TS)底漆用作底物以延伸端粒酶的端粒重复。将延伸产物用该TS引物和Tris-(2'2'-双吡啶基)钌(TBR) - 标记的反相引物扩增。通过链霉蛋白涂覆的磁珠分离并富集电极表面的扩增产物,并通过测量标记的TBR的ECL信号来检测。测量端粒酶活性使用传感器易于,敏感,快速,适用于定量分析,应在临床上用于检测和监测端粒酶活性。

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