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Dual-Utility of Digital Holography & Epi-Fluorescence to Localize Cellular Nuclei.

机译:数字全息图和Epi荧光的双重功能,可定位细胞核。

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摘要

Digital Holographic Microscopy (DHM) and Epi-Fluorescence have been combined for biological imaging. DHM is a non-invasive phase contrast microscopy technique that provides quantitative information such as the variations in refractive index and physical height. 3D physical height and refractive index profiles are imaged for HEK293 and CHO cells. These values and profiles are compared with known values for the sample gathered from literature and other microscopy techniques, including Scanning Electron Microscopy. The measured CHO cellular length is (15.31 +/- 2.60) microm. Localization of cellular nuclei is performed using the Epi-Fluorescence setup and the DNA specific fluorophore DAPI. The fluorescence intensity profile was imaged, where nuclei shape, size, and localization are compared using an A.1 Zeiss Fluorescence Microscope. The CHO cells are comparable with apoptotic cells, where the measured nucleus length is (10.91 +/- 2.27) microm. DHM and Epi-Fluorescence are combined to analyze the physical heights of the cell as well as localize its nucleus. The combination of these techniques are greatly advantageous to understand cellular functions and variability.
机译:数字全息显微术(DHM)和Epi荧光已被结合用于生物成像。 DHM是一种非侵入性相衬显微镜技术,可提供定量信息,例如折射率和物理高度的变化。对HEK293和CHO细胞的3D物理高度和折射率分布图进行了成像。将这些值和轮廓与从文献和其他显微镜技术(包括扫描电子显微镜)收集的样品的已知值进行比较。测得的CHO细胞长度为(15.31 +/- 2.60)微米。使用Epi荧光设置和DNA特异性荧光团DAPI进行细胞核的定位。对荧光强度分布图进行成像,其中使用A.1 Zeiss荧光显微镜比较核的形状,大小和位置。 CHO细胞与凋亡细胞具有可比性,凋亡细胞的细胞核长度为(10.91 +/- 2.27)微米。 DHM和Epi荧光相结合以分析细胞的物理高度以及定位其细胞核。这些技术的组合对于理解细胞功能和可变性非常有利。

著录项

  • 作者

    Sheldrake, Eric.;

  • 作者单位

    Northern Arizona University.;

  • 授予单位 Northern Arizona University.;
  • 学科 Physics General.;Physics Optics.
  • 学位 M.S.
  • 年度 2014
  • 页码 166 p.
  • 总页数 166
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 新闻学、新闻事业;
  • 关键词

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