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Microscope objective for large-angle fluorescence used for rapid detection of single nucleotide polymorphisms in DNA hybridization

机译:大角度荧光显微镜物镜,用于快速检测DNA杂交中的单核苷酸多态性

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A new type of microscope objective is used for the rapid detection of sequence-dependent affinity variations in DNA hybridization. We demonstrate that by performing probe/target hybridization on coverslips at room temperature terminal SNPs (single nucleotide polymorphisms) can be detected within seconds. The study of weak pair interaction, such as the association of very short DNA oligomers, requires the use of high analyte concentrations of both partners to generate a detectable amount of associated pairs. The background of high concentrations of unbound fluorescing analyte can easily hide the low signal of a weakly affine reaction and makes association extremely difficult to detect. Fluorescence detection is a powerful approach to analyze minute amounts of material, even single molecules, but it is usually limited to rather low concentrations. This limitation is now overcome due to the new type of microscope objective, which produces an extremely small detection volume at a water/glass interface.
机译:一种新型的显微镜物镜用于快速检测DNA杂交中依赖序列的亲和力变化。我们证明,通过在室温下在盖玻片上进行探针/靶标杂交,可以在几秒钟内检测到末端SNP(单核苷酸多态性)。对弱对相互作用的研究,例如非常短的DNA低聚物的缔合,要求使用高分析物浓度的两个伙伴来产生可检测量的相关对。高浓度未结合的荧光分析物的背景很容易掩盖弱仿射反应的低信号,使缔合非常难以检测。荧光检测是一种分析微量物质(甚至是单分子)的有力方法,但通常仅限于相当低的浓度。现在,由于新型的显微镜物镜而克服了这一局限,该物镜在水/玻璃界面产生的检测量极小。

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