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Single dye molecules observed by total internal reflection fluorescence microscopy

机译:通过全内反射荧光显微镜观察单一染料分子

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Total internal reflection fluorescence microscopy (TIRFM) was used to image single molecules with evanescent waves. The molecules were excited by an evanescent wave with different intensities. Single molecules were imaged on low-noise high-quantum-yield charge-coupled device (CCD) cameras. Two-step photobleaching behavior was observed. Duration from fluorescent spots appearing to disappearing was counted. The duration was decided by the speed of photobleaching. Peak intensity was counted as exciting intensity change. The proportion relationship between the reciprocal of duration and exciting intensity was obtained. The emitted intensity and duration of fluorescein were compared with GFP. A single molecules emit the same number photons was proved.
机译:使用全内反射荧光显微镜(TIRFM)对e逝波成像的单个分子进行成像。分子被具有不同强度的e逝波激发。单分子在低噪声高量子产率电荷耦合器件(CCD)相机上成像。观察到两步光致漂白行为。计算从出现荧光斑到消失的持续时间。持续时间取决于光漂白的速度。峰强度算作激发强度变化。得到了持续时间的倒数与激发强度之间的比例关系。将荧光素的发射强度和持续时间与GFP进行比较。证明了单个分子发射相同数量的光子。

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