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首页> 外文期刊>Advanced Materials >Nanometer-Scale Patterning of DNA in Controlled Intervals on a Gold-Disk Array Fabricated Using Ideally Ordered Anodic Porous Alumina
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Nanometer-Scale Patterning of DNA in Controlled Intervals on a Gold-Disk Array Fabricated Using Ideally Ordered Anodic Porous Alumina

机译:使用理想有序阳极多孔氧化铝制造的金盘阵列上可控间隔中DNA的纳米级图案

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摘要

Recently, the development of methods for constructing highly ordered structures of biological molecules such as proteins, DNA, and antibodies on a nanometer scale has become an important subject because these methods can lead to the progressive improvement of the function of biodevices. The observation of patterns of biological molecules using conventional optical microscopes is important in the evaluation of the functions of biological molecules. This is due to the feasibility of this method in aqueous environments and to the simplicity of the instrumentation used. In a previous paper, we have reported the fabrication of highly ordered submicro-meter-sized arrays of DNA on an array of regularly sized Au disks using anodic porous alumina. The fluorescence images of fluorescent-dye-labeled DNA with ideally ordered fluorescence spots were obtained using a conventional fluorescence microscope after a hybridization reaction. When the fabrication of nanopatterns of biological molecules was examined using anodic porous alumina, the resolution limit of the optical fluorescence microscope became a serious problem in the observation of the patterns. A reduction in hole diameter was accomplished by decreasing the anodization voltage, which was also accompanied by a decrease in the hole period. As a result, the interval between the patterns of biological molecules fabricated using conventional anodic porous alumina became too small to be resolved by optical microscopy.
机译:近来,开发用于构建纳米级的诸如蛋白质,DNA和抗体的生物分子的高度有序结构的方法的方法已经成为重要的课题,因为这些方法可以导致生物装置的功能的逐步改善。使用常规光学显微镜观察生物分子的图案对于评估生物分子的功能很重要。这是由于该方法在水性环境中的可行性以及所用仪器的简单性。在以前的论文中,我们报道了使用阳极多孔氧化铝在规则尺寸的Au盘阵列上制造高度有序的亚微米级DNA阵列。在杂交反应之后,使用常规荧光显微镜获得具有理想排序的荧光斑点的荧光染料标记的DNA的荧光图像。当使用阳极多孔氧化铝检查生物分子的纳米图案的制造时,光学荧光显微镜的分辨率极限成为观察图案时的严重问题。孔直径的减小是通过降低阳极氧化电压来实现的,这也伴随着孔周期的减少。结果,使用常规阳极多孔氧化铝制造的生物分子的图案之间的间隔变得太小而无法通过光学显微镜分辨。

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