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A New Approach to Detect a Particular DNA Sequence by UV-Immobilization of Its Hybridization Complex with a Highly Specific Probe Resulting from Ligation of a Tandem of Short Oligonucleotides in Solution

机译:通过在溶液中串联一串短寡核苷酸导致的高特异性探针,通过紫外固定化其杂交复合物来检测特定DNA序列的新方法

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摘要

A new approach was proposed for detecting amplified DNA fragments by hybridization with a highly selective oligonucleotide probe obtained by ligation of a tandem of three short oligonucleotides (pN_8 + pN_4 + pN'_8 (Bio)) in solution, with subsequent UV-immobilization of the hybridization product on a nylon membrane and its colorimetric detection with the streptavidin-alkaline phosphatase technique. Owing to the high selectivity of ligation, the 20-mer legation product was detected on a membrane only when it was fully complementary to a template fragment. The results showed that any single-nucleotide substitution in the tetramer-binding site can be localized and identified with the use of all 12 possible tetramers.
机译:提出了一种新方法来检测扩增的DNA片段,该方法是通过与溶液中串联的三个短寡核苷酸(pN_8 + pN_4 + pN'_8(Bio)串联)获得的高选择性寡核苷酸探针杂交,随后将其紫外线固定尼龙膜上的杂交产物,并用抗生蛋白链菌素碱性磷酸酶技术进行比色检测。由于连接的高选择性,仅在膜上与模板片段完全互补时才在膜上检测到20-mer引物产物。结果表明,可以使用所有12种可能的四聚体来定位和鉴定四聚体结合位点中的任何单核苷酸取代基。

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