首页> 外文期刊>Nucleic Acids Research >Detection of a single base exchange in PCR-amplified DNA fragments using agarose gel electrophoresis containing bisbenzimide-PEG.
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Detection of a single base exchange in PCR-amplified DNA fragments using agarose gel electrophoresis containing bisbenzimide-PEG.

机译:使用含双苯甲酰胺-PEG的琼脂糖凝胶电泳检测PCR扩增的DNA片段中的单碱基交换。

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摘要

Using polymerase chain reaction fragments of known sequences derived from isolates of two related fungal species (Verticillium albo-atrum and V. dahliae), simple submarine electrophoresis in agarose gels containing a bisbenzimide-PEG conjugate (Hanse Analytik (H.A.)-Yellow) has been shown to be capable of distinguishing DNA fragments 567 bp long which differ by as little as a single base change. However, only changes affecting bisbenzimide binding sites (which consist of at least four consecutive A/T bases) alter mobility; other changes are ineffective. A second ligand (H.A.-Red) with high G/C specificity is suggested which may be as effective in detecting other sequence changes.
机译:使用已知的序列的聚合酶链反应片段衍生自两个相关真菌物种(黄萎病菌和大叶黄萎病菌)的分离物,已在含有双苯甲酰亚胺-PEG共轭物(Hanse Analytik(HA)-黄色)的琼脂糖凝胶中进行了简单的海底电泳。证明能够区分567 bp长的DNA片段,这些片段相差仅一个碱基改变。但是,只有影响双苯甲酰亚胺结合位点(由至少四个连续的A / T碱基组成)的变化才会改变迁移率;其他更改无效。建议使用具有高G / C特异性的第二个配体(H.A.-Red),它可以有效地检测其他序列变化。

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