In Vivo Two-Photon Laser Scanning Microscopy with Concurrent Plasma-Mediated Ablation Principles and Hardware Realization
In Vivo Two-Photon Laser Scanning Microscopy with Concurrent Plasma-Mediated Ablation Principles and Hardware Realization
复制标题
具有并行等离子体介导消融原理和硬件实现的体内双光子激光扫描显微镜
DOI:
10.1201/9781420076851.ch3
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发表时间:
2009
影响因子:
--
通讯作者:
D. Kleinfeld
中科院分区:
文献类型:
--
作者:
P. Tsai;D. Kleinfeld
Many biological processes of current interest occur below the surface layers of accessible tissue. It is often the case that the surface layers cannot easily be removed without adversely affecting the physiology and function of the deeper layers. A variety of imaging techniques have been developed to perform sectioning deep to the surface using optical, electrical, and magnetic contrast agents and recording methods. Two-photon laser scanning microscopy (TPLSM) with ultrashort (i.e., order 100-fs) pulsed laser light provides optically sectioned images from depths of 500 microns or more below the surface in highly scattering brain tissue [1–5]. This method is unique in that it can provide images with submicrometer lateral resolution and micrometer axial resolution on the millisecond time-scale [6], as is required for the study of many dynamic biological processes [1,7–11].
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3.4
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