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Confocal Imaging using Synchrotron Radiation

机译:使用同步辐射的共聚焦成像

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The physical principles of confocal imaging in conjunction with synchrotron radiation from the 2 Gev synchrotron radiation source (the SRS) at Daresbury Laboratory have been combined in the construction & operation of a uniquely versatile microscope. This scanning microscope is designed primarily for the three dimensional imaging of biological material. The microscope operates at any wavelength in the range from 200 nm to ~ 700 nm and achieves high lateral and axial resolution in the reflection contrast mode which is close to the theoretical limits of λ/3 and λ respectively. The microscope is used to achieve three dimensional imaging by 'optical slicing'; a method which is considerably enhanced in usefulness for biological samples by the ability to simultaneously observe images both with reflection and fluorescence contrast. Recently sample contrast has been obtained using fluorescence polarisation imaging giving information about molecular (probe) orientation within the sample. The microscope is used also in a non scanning mode where a near diffraction limited volume is chosen within an appropriate site within the sample. It is then feasible to undertake "micro volume spectroscopy" and to measure fluorescence lifetime, polarisation, intensity and spectrum as a function of time yielding a powerful armoury of "chemical mapping" techniques to study the internal structures of cells and of membrane transport mechanisms using intrinsic or extrinsic fluorescence probes.
机译:共焦成像的物理原理与来自Daresbury实验室的2 Gev同步加速器辐射源(SRS)的同步加速器辐射相结合,共同构成了独特的多功能显微镜。该扫描显微镜主要设计用于生物材料的三维成像。该显微镜可在200 nm至〜700 nm范围内的任何波长下工作,并在反射对比模式下获得较高的横向和轴向分辨率,分别接近λ/ 3和λ的理论极限。显微镜用于通过“光学切片”实现三维成像。通过同时观察具有反射和荧光对比的图像的能力,大大提高了对生物样品的实用性的方法。最近,已经使用荧光偏振成像获得了样品对比度,该荧光偏振成像给出了有关样品内分子(探针)取向的信息。显微镜还用于非扫描模式,在该模式下,在样品的适当位置内选择了接近衍射极限的体积。然后,可以进行“微体积光谱学”并测量荧光寿命,偏振,强度和光谱随时间的变化,从而产生强大的“化学作图”技术,以研究细胞的内部结构和膜转运机制。内部或外部荧光探针。

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