碱性磷酸酶偶联寡核苷酸探针用于法医DNA分析的特异性评价。

E A Benzinger, A K Riech, R E Shirley, K R Kucharik
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引用次数: 0

摘要

目前法医DNA分析的限制性片段长度多态性分析方法依赖于DNA的放射性检测。放射性同位素的使用既复杂又昂贵,还需要周密的安全防范措施。最近,涉及使用碱性磷酸酶偶联寡核苷酸探针的非放射性检测方法已经成为可能。这些探针不同于大多数32p标记的探针,因为它们是合成的寡核苷酸,而32p标记的探针是从克隆的VNTR区域纯化的质粒插入物。由于这种差异,非同位素探针的特异性可能与32p标记探针的特异性不同。本研究通过对一组DNA样本(包括位于D1S7、D2S44、D4S139、D10S28和D17S26位点的一组相对较小的等位基因)进行平行分析,比较了两种探针的特异性。我们发现,虽然碱性磷酸酶检测方法的灵敏度略低于32P检测方法,但所测试的ap偶联寡核苷酸探针具有与32P标记的质粒插入物相当的特异性,并且是合适的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the specificity of alkaline phosphatase-conjugated oligonucleotide probes for forensic DNA analysis.

Current methods of forensic DNA profiling by restriction fragment length polymorphism analysis rely on radioactive detection of DNA. The use of radioactive isotopes is complicated, expensive and requires elaborate safety precautions. Recently, non-radioactive detection methods involving the use of alkaline phosphatase-conjugated oligonucleotide probes have become available. These probes differ from most 32P-labeled probes in that they are synthetic oligonucleotides, whereas the 32P-labeled probes are purified plasmid inserts from cloned VNTR regions. Because of this difference, it is possible that the specificity of the non-isotopic probe will differ from that of the 32P-labeled probe. This study compares the specificity of the two types of probes by parallel analysis of a set of DNA samples, including a subset of relatively small alleles, at the loci D1S7, D2S44, D4S139, D10S28, and D17S26. We found that although the alkaline phosphatase detection method is slightly less sensitive than 32P detection, the AP-conjugated oligonucleotide probes tested have specificity comparable to, and are appropriate and suitable substitutes for, 32P-labeled plasmid inserts.

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