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Couple polymerase chain reaction - restriction endonuclease digestion - ligase detection reaction method

机译:偶合聚合酶链反应-限制性核酸内切酶消化-连接酶检测反应方法

摘要

The present invention provides a method for identifying one or more low abundance sequences differing by one or more single-base changes, insertions, or deletions, from a high abundance sequence in a plurality of target nucleotide sequences. The high abundance wild-type sequence is selectively removed using high fidelity polymerase chain reaction analog conversion, facilitated by optimal buffer conditions, to create a restriction endonuclease site in the high abundance wild-type gene, but not in the low abundance mutant gene. This allows for digestion of the high abundance DNA. Subsequently the low abundant mutant DNA is amplified and detected by the ligase detection reaction assay. The present invention also relates to a kit for carrying out this procedure.
机译:本发明提供了一种用于鉴定多个靶核苷酸序列中与高丰度序列不同的一个或多个低丰度序列与一个或多个单碱基改变,插入或缺失不同的方法。使用高保真度聚合酶链反应类似物转化,在最佳缓冲液条件下,有选择地去除高丰度野生型序列,以在高丰度野生型基因中创建限制性核酸内切酶位点,而在低丰度突变基因中不产生限制性核酸内切酶位点。这样可以消化高丰度的DNA。随后,通过连接酶检测反应测定法扩增和检测低丰度突变体DNA。本发明还涉及用于执行该过程的试剂盒。

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