superresolution structured illumination microscopy (sr-sim) instrument Search Results


sim microscopy  (Oxford Instruments)
99
Oxford Instruments sim microscopy
Sim Microscopy, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superresolution+structured+illumination+microscopy+(sr-sim)+instrument/Imaris/pm37658339-144-11-17
Average 99 stars, based on 1 article reviews
sim microscopy - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
illumination  (Nikon)
96
Nikon illumination
Properties of single plane <t> illumination </t> microscopy.
Illumination, supplied by Nikon, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superresolution+structured+illumination+microscopy+(sr-sim)+instrument/Illumination+Systems/pmc03941456-87-17-22
Average 96 stars, based on 1 article reviews
illumination - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier
mouse acetylated tubulin primary antibody  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology mouse acetylated tubulin primary antibody
Properties of single plane <t> illumination </t> microscopy.
Mouse Acetylated Tubulin Primary Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superresolution+structured+illumination+microscopy+(sr-sim)+instrument/Tubulin+Antibody/pmc05676932-1023-14-19
Average 96 stars, based on 1 article reviews
mouse acetylated tubulin primary antibody - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier

Image Search Results


Properties of single plane illumination microscopy.

Journal: The Yale Journal of Biology and Medicine

Article Title: Fluorescence Microscopy Gets Faster and Clearer: Roles of Photochemistry and Selective Illumination

doi:

Figure Lengend Snippet: Properties of single plane illumination microscopy.

Article Snippet: Commercial systems are available from Leica, albeit the utility of other ensemble superresolution systems based on structured illumination are available from both Nikon (N-SIM/N-STORM) and Zeiss (SR-SIM) and may be better suited for multi-user facilities.

Techniques: Microscopy, Fluorescence, Confocal Microscopy

Single plane illumination microscopy (SPIM) light path in the Zeiss Lightsheet Z.1 microscope (light sheet fluorescence microscopy: LSFM) using a whole zebrafish embryo. Illumination lenses (black), detection objective: W Plan-APHCHORMAT 20x/1.0 (white), lightsheet (blue). LSFM separates fluorescence excitation and detection into two separate light paths, with the axis of sheet illumination orthogonal to the detection axis (green). Laser light is focused into a thin light sheet by cylindrical lenses (not shown) upstream of the illuminating objectives. Only the in-focus light sheet excites fluorescence, significantly reducing phototoxicity. Use of two oppositional illuminating objectives reduces shadowing artifacts and increases acquisition speed. Fluorescence is collected on ultrafast CMOS cameras enabling z-stack acquisition speeds >100-fold faster than laser scanning confocal microscopy. Image courtesy of Carl Zeiss Microscopy GmbH. Used with permission.

Journal: The Yale Journal of Biology and Medicine

Article Title: Fluorescence Microscopy Gets Faster and Clearer: Roles of Photochemistry and Selective Illumination

doi:

Figure Lengend Snippet: Single plane illumination microscopy (SPIM) light path in the Zeiss Lightsheet Z.1 microscope (light sheet fluorescence microscopy: LSFM) using a whole zebrafish embryo. Illumination lenses (black), detection objective: W Plan-APHCHORMAT 20x/1.0 (white), lightsheet (blue). LSFM separates fluorescence excitation and detection into two separate light paths, with the axis of sheet illumination orthogonal to the detection axis (green). Laser light is focused into a thin light sheet by cylindrical lenses (not shown) upstream of the illuminating objectives. Only the in-focus light sheet excites fluorescence, significantly reducing phototoxicity. Use of two oppositional illuminating objectives reduces shadowing artifacts and increases acquisition speed. Fluorescence is collected on ultrafast CMOS cameras enabling z-stack acquisition speeds >100-fold faster than laser scanning confocal microscopy. Image courtesy of Carl Zeiss Microscopy GmbH. Used with permission.

Article Snippet: Commercial systems are available from Leica, albeit the utility of other ensemble superresolution systems based on structured illumination are available from both Nikon (N-SIM/N-STORM) and Zeiss (SR-SIM) and may be better suited for multi-user facilities.

Techniques: Microscopy, Fluorescence, Confocal Microscopy