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Two-Point Separation in Far-Field Super-Resolution Fluorescence Microscopy Based on Two-Color Fluorescence Dip Spectroscopy, Part I: Experimental Evaluation

机译:基于双色荧光浸没光谱的远场超高分辨率荧光显微镜中的两点分离,第一部分:实验评估

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The two-point resolution of a novel two-color far-field super-resolution fluorescence microscopy was evaluated by measuring fluorescent beads 100 nm in diameter. This microscopy is based on a combination of two-color fluorescence dip spectroscopy and a phase-modulation technique for a laser beam. By simply introducing two-color laser light, the size of the fluorescent image of a bead was shrunk down to a diameter of 250 nm from the diffraction-limited image with a diameter of 360 nm. For two closely adjacent fluorescent beads with a separation distance of 350 nm, the two-color microscope clearly gave separated fluorescence images, while the conventional one-color fluorescence microscope could not resolve them. It has been proved that our technique breaks Rayleigh's diffraction limit.
机译:通过测量直径为100 nm的荧光珠来评估新型两色远场超分辨率荧光显微镜的两点分辨率。该显微镜基于双色荧光浸没光谱法和激光束的相位调制技术的结合。通过简单地引入两种颜色的激光,珠子的荧光图像的尺寸从直径为360nm的衍射极限图像缩小到直径为250nm。对于分离距离为350 nm的两个紧密相邻的荧光珠,两色显微镜清楚地给出了分离的荧光图像,而常规的一色荧光显微镜无法分辨它们。事实证明,我们的技术突破了瑞利的衍射极限。

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