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首页> 外文期刊>Journal of Fluorescence >Detection of Single Quantum Dots in Model Systems with Sheet Illumination Microscopy
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Detection of Single Quantum Dots in Model Systems with Sheet Illumination Microscopy

机译:用纸张照明显微镜检测模型系统中的单量子点

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摘要

Single molecule detection and tracking provides at times the only possible method to observe the interactions of low numbers of biomolecules, inlcuding DNA, receptors and signal mediating proteins in living systems. However, most existing imaging methods do not enable both high sensitivity and non-invasive imaging of large specimens. In this study we report a new setup for selective plane illumination microscopy (SPIM), which enables fast imaging and single molecule tracking with the resolution of confocal microscopy and the optical penetration beyond 300 mu m. We detect and report our instrumental figures of merit, control values of fluorescence properties of single nano crystals in comparison to both standard widefield configurations, and also values of nanocrystals in multicellular "fruiting bodies" of Dictyostelium, an excellent control as a model developmental system. In the Dictyostelium , we also report some of our first tracking of single nanocrystals with SPIM. The new SPIM setup represents a new technique, which enables fast single molecule imaging and tracking in living systems.
机译:单分子检测和跟踪有时提供唯一可能的方法,观察较低数量的生物分子的相互作用,嵌入DNA,受体和在活生植物中介导蛋白质中的蛋白质。然而,大多数现有的成像方法都不能够实现大型样本的高灵敏度和非侵入性成像。在这项研究中,我们报告了一种用于选择性平面照明显微镜(SPIM)的新设置,其能够通过共聚焦显微镜的分辨率和超出300μm的光学穿透的快速成像和单分子跟踪。我们检测并报告我们的乐器图,单个纳米晶体的荧光特性的荧光性质的控制值与标准宽泛的配置相比,以及Dictyostelium的多细胞“结果体”中的纳米晶体的值,作为模型发育系统的优异控制。在Dictyostelium中,我们还报告了我们的首次跟踪单个纳米晶体与尖端。新的SPIM设置代表了一种新技术,它能够快速单分子成像和在生活系统中跟踪。

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