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Hyperspectral backscatter imaging: a label-free approach to cytogenetics

机译:高光谱背散射成像:细胞遗传学的无标记方法

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摘要

Current techniques for chromosome analysis need to be improved for rapid, economical identification of complex chromosomal defects by sensitive and selective visualisation. In this paper, we present a straightforward method for characterising unstained human metaphase chromosomes. Backscatter imaging in a dark-field setup combined with visible and short near-infrared spectroscopy is used to monitor morphological differences in the distribution of the chromosomal fine structure in human metaphase chromosomes. The reasons for the scattering centres in the fine structure are explained. Changes in the scattering centres during preparation of the metaphases are discussed. FDTD simulations are presented to substantiate the experimental findings. We show that local scattering features consisting of underlying spectral modulations of higher frequencies associated with a high variety of densely packed chromatin can be represented by their scatter profiles even on a sub-microscopic level. The result is independent of the chromosome preparation and structure size. This analytical method constitutes a rapid, cost-effective and label-free cytogenetic technique which can be used in a standard light microscope.
机译:需要改进当前的染色体分析技术,以便通过灵敏和选择性的可视化快速,经济地识别复杂的染色体缺陷。在本文中,我们提出了一种表征未染色的人类中期染色体的直接方法。暗场设置中的反向散射成像结合可见光和短时近红外光谱用于监测人类中期染色体中染色体精细结构分布的形态学差异。解释了在精细结构中散射中心的原因。讨论了在准备中期过程中散射中心的变化。提出了FDTD仿真,以证实实验结果。我们表明,由与较高浓度的密集染色质相关的较高频率的潜在频谱调制组成的局部散射特征,即使在亚显微水平上也可以由其散射曲线表示。结果与染色体制备和结构大小无关。这种分析方法构成了一种可用于标准光学显微镜的快速,经济,无标签的细胞遗传学技术。

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