Confocal Laser Scanning Imaging A Line Objectives and the FV3000 Microscope/IXplore
Silicone Immersion Objectives
Silicone immersion objectives are optimized for live cell and live tissue imaging. By properly matching the refractive index, images are clearer and brighter, and time−lapse observations become more reliable and less complex because silicone oil does not dry at 37 °C (98.6 ℉). Because the refractive index of silicone immersion oil (ne=1.40) is close to that of the clearing reagent SCALEVIEW–A2 (ne=1.38), the silicone immersion objectives are also well suited for observing SCALEVIEW–A2 cleared samples.


Sample: ScaleA2–treated neocortex, VGluT1/Green, VGluT2/Red, MAP2/Blue
Silicone Versus Oil Immersion 60X Objectives
By matching the refractive index of the sample and immersion medium, the A Line silicone objective (UPLSAPO60XS2) enables deeper imaging.
Image data courtesy of Motokazu Uchigashima, M.D., Ph.D., Masahiko Watanabe, M.D., Ph.D.,
Departments of Anatomy, Hokkaido University Graduate School of Medicine
Three-Dimensional Observation of the Biliary Tree Structure in Mouse Livers with a 30x Objective (UPLSAPO30XS)
The biliary tree structures were compared between Klf5-LKO mice and control mice. Consecutive tomographic images (Z axial interval of 1 μm) of biliary tissue (green, biliary epithelial cell marker CK19) in liver tissue specimens with 200 μm thickness cleared with SeeDB were obtained using the FV3000 and 30x silicone oil immersion objective, enabling high-resolution observation while maintaining a wide field of view. In Klf5-LKO mice, CK19+ cell clusters (white arrow) that were spatially separated from the biliary tree were observed.
Silicone Immersion Objectives Selection Guide
(mm)
*Maximum field number observable through eyepiece.
Super-Corrected 60X Objectives


Better Imaging Performance with a Super-Corrected Chromatic Aberration and a High Numerical Aperture
Colocalized fluorescent signals are a problem that require an objective with a superior optical design to correct for color shifts (aberration). The high numerical aperture super-corrected 60X objective minimizes chromatic aberration to the utmost limit in the 405–650 nm spectrum. 0.1 μm or less axial chromatic aberration is provided in this range, and every objective is delivered with its measured data sheet. This objective can acquire 2D and 3D images with excellent reliability, accuracy, and improved colocalization analysis. Save time and resources in multicolor labeling experiments without having to go through post-processing adjustments.
Super-Corrected 60X Objectives Specifications
(mm)
*Maximum field number observable through eyepiece.
Related Products
FV3000
https://main--eds-evident-website--evident-scientific.hlx.live/en/laser-scanning/fv3000/
- Available with galvanometer-only (FV3000) or hybrid galvanometer/resonant (FV3000RS) scanner configurations
- Efficient, accurate TruSpectral detection on all channels
- Optimized for live-cell imaging with high sensitivity and low phototoxicity
IXplore Spin
https://main--eds-evident-website--evident-scientific.hlx.live/en/landing/ixplore/ixplore-spin/
- Rapid and high-resolution confocal imaging with a spinning disk system
- 3D confocal time-lapse imaging of live cells with less phototoxicity and bleaching
- Precise 3D imaging with improved light collection using silicone oil immersion objectives
- Upgrade to the IXplore SpinSR super resolution system depending on your research progress and/or budget
IXplore SpinSR
https://main--eds-evident-website--evident-scientific.hlx.live/en/landing/ixplore/ixplore-spinsr/
- Super resolution down to 120 nm XY resolution
- Prolonged cell viability in confocal time-lapse imaging due to less phototoxicity and bleaching
- Switch between widefield, confocal, and super-resolution observations in the IXplore SpinSR system in one step
- Accurate 3D reconstruction with Olympus silicone oil immersion objectives
*Banner Image: By courtesy of
Division of Mammalian Development, Genetic Strains Research Center, National Institute of Genetics, Dr. Hajime Okada
Laboratory of Stem Cell Therapy, Institute for Quantitative Biosciences, The University of Tokyo, Project Associate Professor, Dr. Tohru Itoh