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Sub-Diffraction Resolution CARS Microscopy via Rabi Modulation - a Theoretical Investigation

机译:通过Rabi调制进行次衍射分辨率轿厢显微镜 - 理论调查

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Optical microscopy is the modern workhorse of biology, providing high contrast images, often in real time of biological processes at sub-cellular distance scales. Nevertheless, improved understanding of biological processes is difficult to achieve with diffraction-limited resolution as is offered by standard optical microscopy techniques. Sub-diffraction limited resolution has been achieved by two notable techniques: stimulated emission depletion (STED) microscopy [1], and stochastic optical reconstruction microscopy (STORM) [2], but a significant disadvantage of both approaches is that they require chemically attached fluorescent labels in the sample.
机译:光学显微镜是生物学的现代主控,提供高对比度图像,通常在亚蜂窝距离尺度的生物过程的实时。然而,通过标准光学显微镜技术提供的衍射限制分辨率,难以实现对生物过程的改进理解。通过两种值得注意的技术实现了亚衍射有限的分辨率:刺激的发射耗尽(STED)显微镜[1],以及随机光学重建显微镜(风暴)[2],但两种方法的显着缺点是它们需要化学附着的荧光标签在样品中。

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