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Related Concept Videos

Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

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...
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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 developed.
Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
Overview of Microscopy Techniques01:22

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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...
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

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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Phase Contrast and Differential Interference Contrast Microscopy

Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...

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Quantitative Analysis of Autophagy using Advanced 3D Fluorescence Microscopy
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Published on: May 3, 2013

Microscope with enhanced depth of field and 3-d capability.

J S Courtney-Pratt, R L Gregory

    Applied Optics
    |February 4, 2010
    PubMed
    Summary

    Researchers developed a novel microscope objective that enhances depth of field by focusing spectral colors at different distances. This innovation enables sharp 3-D image displays with adjustable depth magnification.

    Area of Science:

    • Microscopy
    • Optical Engineering
    • 3-D Imaging

    Background:

    • Traditional microscope objectives aim for achromatism, focusing all spectral colors at a single point.
    • Increasing the depth of field in microscopy is crucial for detailed 3-D visualization.

    Purpose of the Study:

    • To explore a novel approach for increasing the effective depth of field in microscopy.
    • To enable 3-D image viewing by utilizing differential spectral color focusing.

    Main Methods:

    • Designed a microscope objective that intentionally deviates from achromatism, causing spectral colors to focus at different distances.
    • Modified a binocular eyepiece to adjust image convergence based on spectral color.
    • Developed a 16-mm NA 0.4 objective achieving 1-micrometer lateral resolution and 100-micrometer depth of field.

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    Super-resolution Imaging of the Cytokinetic Z Ring in Live Bacteria Using Fast 3D-Structured Illumination Microscopy (f3D-SIM)
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    Super-resolution Imaging of the Cytokinetic Z Ring in Live Bacteria Using Fast 3D-Structured Illumination Microscopy (f3D-SIM)
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    Main Results:

    • Demonstrated a microscope objective with an extended depth of field.
    • Achieved a lateral resolution of 1 micrometer and a depth of field of 100 micrometers.
    • Developed 3-D displays capable of presenting sharp images with variable depth magnification up to +/- 40,000x.

    Conclusions:

    • The proposed method effectively increases the depth of field in microscopy.
    • This technique allows for high-resolution 3-D imaging with adjustable depth magnification.
    • The developed objective and display system offer significant advancements in microscopic visualization.