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Atomic force microscopy and scanning near-field optical microscopy studies on the characterization of human metaphase chromosomes

机译:原子力显微镜和扫描近场光学显微镜研究人类中期染色体的特征

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摘要

A better knowledge of biochemical and structural properties of human chromosomes is important for cytogenetic investigations and diagnostics. Fluorescence in situ hybridization (FISH) is a commonly used technique for the visualization of chromosomal details. Localizing specific gene probes by FISH combined with conventional fluorescence microscopy has reached its limit. Also, microdissecting DNA from G-banded human metaphase chromosomes by either a glass tip or by laser capture needs further improvement. By both atomic force microscopy (AFM) and scanning near-field optical microscopy (SNOM), local information from G-bands and chromosomal probes can be obtained. The final resolution allows a more precise localization compared to standard techniques, and the extraction of very small amounts of chromosomal DNA by the scanning probe is possible. Besides new strategies towards a better G-band and fluorescent probe detection, this study is focused on the combination of biochemical and nanomanipulation techniques which enable both nanodissection and nanoextraction of chromosomal DNA.
机译:更好地了解人类染色体的生化和结构特性对于细胞遗传学研究和诊断很重要。荧光原位杂交(FISH)是用于可视化染色体细节的常用技术。通过FISH结合常规荧光显微镜对特定基因探针进行定位已达到其极限。同样,通过玻璃尖端或激光捕获从G带人类中期染色体上将DNA进行显微解剖还需要进一步改进。通过原子力显微镜(AFM)和扫描近场光学显微镜(SNOM),可以获得来自G波段和染色体探针的局部信息。与标准技术相比,最​​终分辨率可以实现更精确的定位,并且可以通过扫描探针提取非常少量的染色体DNA。除了更好的G波段和荧光探针检测的新策略外,本研究的重点还在于结合生化和纳米处理技术,使染色体DNA的纳米切割和纳米提取成为可能。

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