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通过辅助光纤光收集增强非线性显微镜中的荧光信号。

Enhanced fluorescence signal in nonlinear microscopy through supplementary fiber-optic light collection.

作者信息

Engelbrecht Christoph J, Göbel Werner, Helmchen Fritjof

机构信息

Department of Neurophysiology, Brain Research Institute, University of Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.

出版信息

Opt Express. 2009 Apr 13;17(8):6421-35. doi: 10.1364/oe.17.006421.

Abstract

Nonlinear microscopy techniques crucially rely on efficient signal detection. Here, we present a ring of large-core optical fibers for epi-collection of fluorescence photons that are not transmitted through the objective and thus normally wasted. Theoretical treatments indicated that such a supplementary fiber-optic light collection system (SUFICS) can provide an up to 4-fold signal gain. In typical in vivo imaging experiments, the fiber-ring channel was brighter than the objective channel down to 800 microm depth, thus providing a gain >2. Moreover, SUFICS reduced noise levels in calcium imaging experiments by about 23%. We recommend SUFICS as a generally applicable, effective add-on to nonlinear microscopes for enhancing fluorescence signals.

摘要

非线性显微镜技术在很大程度上依赖于高效的信号检测。在此,我们展示了一种用于落射收集荧光光子的大芯光纤环,这些荧光光子不会透过物镜,因此通常会被浪费掉。理论分析表明,这种辅助光纤光收集系统(SUFICS)可提供高达4倍的信号增益。在典型的体内成像实验中,光纤环通道在深度达800微米时比物镜通道更亮,因此增益大于2。此外,SUFICS在钙成像实验中将噪声水平降低了约23%。我们推荐SUFICS作为非线性显微镜的一种普遍适用且有效的附加装置,用于增强荧光信号。

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