首页> 外文会议>Engineering in Medicine and Biology Society, 2003. Proceedings of the 25th Annual International Conference of the IEEE >Fast laser-scanning microscopy with single- and multi-photon excitation for functional imaging of living nerve cells
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Fast laser-scanning microscopy with single- and multi-photon excitation for functional imaging of living nerve cells

机译:具有单光子和多光子激发的快速激光扫描显微镜,用于活神经细胞的功能成像

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Functional neuro-imaging is often limited by the spatio-temporal resolution of available imaging systems. The goal of this project is fast multi-site imaging of nerve cells in intact mammalian brain tissue. We will review fundamentals of fast laser-scanning microscopy employing acousto-optic beam steering and show examples of neuro-imaging applications. Specifically, we will discuss the significance and technical challenges of extending this imaging approach from single- to multi-photon excitation. We will present the current development status of a new imaging system implementing acousto-optical scanning of ultra-fast laser pulses.
机译:功能性神经成像通常受可用成像系统的时空分辨率限制。该项目的目标是对完整的哺乳动物脑组织中的神经细胞进行快速的多部位成像。我们将回顾采用声光光束控制的快速激光扫描显微镜的基础知识,并展示神经成像应用的示例。具体而言,我们将讨论将这种成像方法从单光子激发扩展到多光子激发的意义和技术挑战。我们将介绍实现超快激光脉冲声光扫描的新成像系统的当前发展状况。

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