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METHOD FOR DETECTING MUTATIONS, INSERTIONS, DELETIONS AND POLYMORPHISMS ON DNA AND THE USE THEREOF

机译:检测DNA上的突变,插入,缺失和多态性的方法及其用途

摘要

The inventive method for detecting mutations, insertions, deletions and polymorphisms on DNA is characterized in that a first specific PCR reaction is carried out with a primer pair which flanks the position of the genome which is to be examined, wherein a respectively different universal oligonucleotide sequence, which is not complementary with the DNA sequence to be examined, is also joined to the 5'-end of each primer; a second universal PCR reaction is carried out with a marked primer pair which is complementary to the universal oligonucleotide sequences used in the first PCR.
机译:用于检测DNA上的突变,插入,缺失和多态性的本发明方法的特征在于,用侧接待检查基因组位置的引物对进行第一特异性PCR反应,其中分别具有不同的通用寡核苷酸序列与待检查的DNA序列不互补的DNA,也连接到每个引物的5'末端;用标记的引物对进行第二次通用PCR反应,该引物对与第一次PCR中使用的通用寡核苷酸序列互补。

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