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Confocal Laser Scanning Imaging


Laser scanning microscopy (LSM) is used to obtain high-resolution, high-contrast imagery of a sample. LSM can scan samples point by point, resulting in optical sectioning that can be used to construct precise 3D images.
Olympus X Line objective lenses boost the performance of LSM with increased numerical aperture (NA) for higher resolution, increased chromatic correction for better colocalization experiments, and better flatness for excellent mosaic imaging results.

Discover Your Sample’s True 3D Form

High Resolution and Large Field of View from a Single Objective

Cover a magnification range from 40X to 100X without changing objectives using a 40X, 1.4 NA X Line objective and the FV3000 microscope's optical zoom.

Better Stitching in Multicolor Panoramic Images

Improved image flatness enables you to acquire superior stitched images with less zooming in a wide wavelength range from 400 to 1000 nm.

Brain section of Fucci2 transgenic mouse
Stitched image of 12 × 12 images acquired by an FV3000 using a 60X oil immersion objective (NA1.42)
Cyan: DAPI (405 nm) Magenta: mCherry (561 nm)
Image Courtesy of: Laboratory for Cell Function Dynamics, RIKEN Center for Brain Science
Takako Kogure, Atsushi Miyawaki

Comparaison d'objectifs conventionnels (à gauche) avec les objectifs X Line (à droite)
Comparaison d'objectifs conventionnels (à gauche) avec les objectifs X Line (à droite)
Aberration chromatique axiale
À gauche : objectifs conventionnels /  À droite : X Line
À gauche : objectifs conventionnels /  À droite : X Line
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True Colocalization Analysis

X Line objective’s chromatic aberration correction from 400 to 1000 nm is the basis for accurate quantitative colocalization analysis. Trust what you see—only with X Line objectives can you can be sure that two signals really colocalize, as insufficient chromatic correction can easily introduce a shift of fluorescence channels in the Z dimension.

Image: HeLa cell labeled by FISH technique  CEP17(Spectrum Green), CEP18(Spectrum Orange), Nuclear (DAPI)*

When observing with conventional objectives, signals located at the bottom of the cell’s nucleus appear outside the nucleus. Scale bar: 2 μm

See the True 3D Shape of Your Sample with Silicone Immersion Objectives

Matching the refractive index of a sample and immersion media is very important to get accurate 3D images. Mismatches of refractive indices (water or standard immersion oil) will lead to distortions of the 3D image. Only silicone immersion oil provides the right refractive index of living samples and results in true 3D images. Olympus’ A Line silicone oil objectives enable you to see the truth in your 3D samples.


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