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USE OF METHOD FOR THE DETECTION OF MULTIPLE TARGET NUCLEIC ACIDS USING CLAMPING PROBES AND DETECTION PROBES

机译:利用钳位问题和检测问题检测多目标核酸的方法的使用

摘要

The present invention relates to application of a target nucleic acid detection method using a clamping probe and a detection probe. According to the present invention, wild-type genes or amplification of undesired genes is prevented; an ultra-small amount of a target gene to be detected can be selectively amplified and detected; and consequently a small amount of mutation or a certain gene sequence included in a sample can be effectively detected. In addition, a large amount of gene types can be simultaneously detected by melting curve analysis. In particular, the target nucleic acid detection method can be used as a method for assisting medical diagnosis and prognosis of diseases, monitoring diseases, evaluating a treatment effect, and researching delivery of nucleic acid and protein by using an ultra-small amount of mutant genotype which can be detected at high detection sensitivity. The target nucleic acid detection method includes a step of detecting biomarkers such as EGFR, KRAS, NRAS and so on and determining whether a mutant of the biomarker exists by using a sample such as tissue, obtained by an invasive method, but also a sample such as blood, urine, sputum, excrement, saliva, and cells obtained by a non-invasive method. The biomarker and the mutant are used to monitor all periods of related diseases, prognose diseases, predict diseases, determine a treatment for diseases, diagnose diseases or diagnose disease early, prevent diseases, and develop a treating agent for diseases.
机译:本发明涉及使用夹持探针和检测探针的靶核酸检测方法的应用。根据本发明,防止了野生型基因或不希望的基因的扩增。可以选择性地扩增和检测极少量的待检测靶基因。因此可以有效地检测出样品中少量的突变或某种基因序列。另外,可以通过解链曲线分析同时检测大量基因类型。特别地,靶核酸检测方法可以用作通过使用超少量的突变基因型来辅助疾病的医学诊断和预后,监测疾病,评估治疗效果以及研究核酸和蛋白质的输送的方法。可以高检测灵敏度进行检测。靶核酸检测方法包括以下步骤:检测诸如EGFR,KRAS,NRAS等的生物标记,并通过使用通过侵入性方法获得的诸如组织的样本来确定是否存在该生物标记的突变体,并且还包括诸如如通过非侵入性方法获得的血液,尿液,痰,排泄物,唾液和细胞。生物标志物和突变体用于监测所有时期的相关疾病,预测疾病,预测疾病,确定疾病的治疗方法,及早诊断疾病或诊断疾病,预防疾病以及开发疾病治疗剂。

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