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Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
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Confocal Fluorescence Microscopy01:16

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Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
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The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
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Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
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Phase-Contrast Microscopes
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Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
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  1. ホーム
  2. オプティカルイメージング. 膨張顕微鏡による顕微鏡
  1. ホーム
  2. オプティカルイメージング. 膨張顕微鏡による顕微鏡

関連する実験動画

Author Spotlight: Universal Molecular Retention with 11-Fold Expansion Microscopy
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オプティカルイメージング. 膨張顕微鏡による顕微鏡

Fei Chen1, Paul W Tillberg2, Edward S Boyden3

  • 1Department of Biological Engineering, Massachussetts Institute of Technology (MIT), Cambridge, MA, USA.

Science (New York, N.Y.)
|January 17, 2015

PubMed で要約を見る

まとめ
この要約は機械生成です。

膨張顕微鏡 (ExM) は,膨張性ポリマーネットワークを合成することによって,物理的に標本を拡大します. この技術は, ~70 nm の解像度を達成するために,従来の difraktion-limited 顕微鏡でスケーラブルな超解像度イメージングを可能にします.

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科学分野:

  • バイオフィジックス 生物物理学
  • 光学顕微鏡による光学顕微鏡です.
  • 材料科学 材料科学とは

背景:

  • 光学顕微鏡は,画像の拡大のために屈折に依存しています.
  • 細かい構造的な詳細は,しばしば光学 difraktion 制限によって制限されます.

研究 の 目的:

  • 微分光差制限器具を使用して,スケーラブルな超解像度顕微鏡のための方法を開発する.
  • 生物イメージングの光学微分極限の限界を克服するために.

主な方法:

  • 生物標本内で膨らむポリマーネットワークを合成する.
  • ポリマーネットワークにコーバル的にラベルを固定し,同otropic 拡張を可能にします.
  • ポリマーネットワークの拡張を介して物理的な拡大を使用します.

主要な成果:

  • ~70ナノメートルの横断解像度を持つ拡張顕微鏡 (ExM) を実証しました.
  • 培養細胞と脳組織で超高解像度イメージングを達成しました.
  • コンフォカル顕微鏡を用いてマウスの海馬の3色超高解像度イメージングを行った.

結論:

  • ExMは,従来の顕微鏡でスケーラブルな超解像度顕微鏡を可能にします.
  • 物理的な膨張は,高解像度のために光学屈折の限界を克服します.
  • ExMは,生物学的構造の高解像度イメージングのための強力な技術です.