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関連する概念動画

Plant Tissues01:18

Plant Tissues

Plants are multicellular eukaryotes with tissue systems made of various cell types that carry out specific functions. Different tissues work together to perform a unique function and form an organ. Organs working together form organ systems. Vascular plants have two distinct organ systems: a shoot system and a root system. The shoot system consists of two portions: the vegetative (non-reproductive) parts of the plant, such as the leaves and the stems, and the reproductive parts of the plant,...
Overview of Electron Microscopy01:25

Overview of Electron Microscopy

The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
Scanning Electron Microscopy01:07

Scanning Electron Microscopy

A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
Fundamental Principles
Accelerated...
Preparation of Samples for Electron Microscopy01:20

Preparation of Samples for Electron Microscopy

To be visualized by an electron microscope, either transmission or scanning, biological samples need to be fixed (stabilized) so the electron beam does not destroy them and dried thoroughly (desiccated/dehydrated) so the vacuum does not affect them. Fixation needs to be done as quickly as possible because the sample properties will start changing as soon as it is removed from its natural environment. For example, in a tissue sample, the oxygen levels begin decreasing, causing an altered...
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

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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関連する実験動画

Updated: Jul 14, 2026

Long-term, High-resolution Confocal Time Lapse Imaging of Arabidopsis Cotyledon Epidermis during Germination
12:01

Long-term, High-resolution Confocal Time Lapse Imaging of Arabidopsis Cotyledon Epidermis during Germination

Published on: December 31, 2012

発達中の植物器官のスキャニング電子顕微鏡検査

R H Falk, E M Gifford, E G Cutter

    Science (New York, N.Y.)
    |June 19, 1970
    PubMed
    まとめ

    植物の発芽アピスと若い葉の直接スキャニング電子顕微鏡は,サンプル準備なしで細胞組織と葉の配置の前例のない可視化を提供します. この方法は,以前見られなかった植物形態学の複雑な詳細を明らかにします.

    科学分野:

    • 植物生物学 植物生物学
    • 顕微鏡による顕微鏡検査
    • モルフォゲネシス (Morphogenesis) モルフォゲネシスとは

    背景:

    • スキャン電子顕微鏡 (SEM) の伝統的な方法は,固定と金属コーティングを含む広範なサンプル準備を必要とします.
    • これらの準備段階は,人工物を導入し,繊細な生物標本の細かい構造の詳細を曖昧にすることができます.

    研究 の 目的:

    • 植物のシューティングアピスと若いメリステマティック葉の直接的なSEMイメージングの実現可能性を調査する.
    • アーティファクトを誘発する準備ステップなしで植物形態の観察の可能性を実証する.

    主な方法:

    • スキャニング電子顕微鏡を用いたショットアピスと若いメリステマティック葉の直接検査.
    • サンプルには,先行固定または金属コーティングの手順が適用されていません.

    主要な成果:

    • ショット・アペックス・フォーム,細胞組織,葉の配置 (フィロタクシス) の視覚化が成功しました.
    • 高解像度画像は,植物構造の複雑な詳細を明らかにしました.
    • 直接的なイメージングアプローチは,標本の自然な状態を保ちました.

    結論:

    さらに関連する動画

    Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces
    07:01

    Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces

    Published on: May 22, 2018

    Confocal Live Imaging of Shoot Apical Meristems from Different Plant Species
    06:46

    Confocal Live Imaging of Shoot Apical Meristems from Different Plant Species

    Published on: March 29, 2019

    関連する実験動画

    Last Updated: Jul 14, 2026

    Long-term, High-resolution Confocal Time Lapse Imaging of Arabidopsis Cotyledon Epidermis during Germination
    12:01

    Long-term, High-resolution Confocal Time Lapse Imaging of Arabidopsis Cotyledon Epidermis during Germination

    Published on: December 31, 2012

    Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces
    07:01

    Development of Microfluidic Devices to Study the Elongation Capability of Tip-growing Plant Cells in Extremely Small Spaces

    Published on: May 22, 2018

    Confocal Live Imaging of Shoot Apical Meristems from Different Plant Species
    06:46

    Confocal Live Imaging of Shoot Apical Meristems from Different Plant Species

    Published on: March 29, 2019

    • 直接的なSEMは,植物の芽と若い葉を研究するための実行可能で強力な技術です.
    • この方法は,植物形態変異と発達に関する新しい洞察を提供します.
    • これは,最小限の人工物で繊細な植物構造を視覚化するための重要な進歩を提供します.