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Super Resolution Microscopes

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Abberior Facility Line STED Microscope

Abberior Facility Line STED MicroscopeAbberior Facility Line STED Microscope

  • Super-resolution STED microscope capable of lateral resolution ~40 nm and axial resolution ~80 nm.
  • Suitable for super-resolution imaging in cultured cells, tissue slices, and other preparations.
  • Fluorescence Lifetime Imaging (FLIM) for FRET and other new measurements.
  • Core hardware for image acquisition
      • Laser lines: 405, 485, 561 and 640 nm for imaging and a pulsed STED laser at 775nm.
      • Detection via 3 photon-counting APDs and 1 Matrix detector for effective removal of background signals.
      • Inverted Olympus IX83 with 10x (dry), 20x (dry), 40x (dry), 60x (silicone oil) and 60x (oil) objectives for a broad range of applications, motorized stage, and Z drift compensation.
  • Capable of imaging fixed and live samples.
      • Okolab stage-top incubator for temperature and CO2 control for live-cell imaging.
      • A range of sample holders is available.
      • STED-capable live-cell stains are available for a variety of intracellular targets.
  • Unique accessories to increase resolution, decrease photobleaching, and:
      • Adaptive optics to correct for spherical aberrations and compensate for sample-induced aberrations.
      • Adaptive Illumination that facilitates high resolution and low-light gentle imaging of live-cells.
      • Novel approaches called DyMIN and RESCue that reduce the total light power delivered to the sample during image scanning.

 

Applications

  • Nanoscale Super-Resolution Imaging (STED) facilitating resolution down to 30–50 nm. Enables visualization of sub-diffraction structures like cytoskeleton (actin, microtubules), synaptic vesicles and organelle sub-compartments.
  • Time-Resolved & Lifetime-Enhanced Imaging (Time-Bin / Gating) improves resolution and contrast by filtering the background, enabling lifetime-based separation of signals, and also can reduce autofluorescence and enhance signal specificity.
  • Deep Tissue & Aberration-Corrected Imaging using the adaptive optics.
  • Live-Cell STED Imaging (Advanced Applications) 

Zeiss LSM 880 with Airyscan

Zeiss LSM 880 with Airyscan

  • Point scanning confocal on an upright Zeiss Examiner microscope stand.
  • Offers high sensitivity, enhanced resolution in x, y and z and high image-acquisition speed.
  • Equipped with Zeiss Airyscan and Fast Airyscan detector, which can improve the signal to noise ratio (4-8x) and increase resolution 1.7x
  • Definite Focus to prevent focal drift.
  • Equipped with 7 laser lines (355, 458/488/514 nm (Argon), 561 nm, 594 nm, and 633 nm) and a motorized stage and software for automated tiling and stitching.
  • A 34-channel GaAsP-PMT array detector enables precise spectral imaging.
  • Wide range of objective lenses to meet diverse imaging needs in biological research.

 

Applications

  • Superresolution Imaging with the Airyscan provides a lateral resolution of about 140nm and an axial resolution of 400nm. 
  • Tile scanning of large tissue section samples.

Nikon NSTORM

Nikon NSTORM

The Nikon NSTORM microscope can perform STORM, DNA-PAINT, and TIRF imaging along with correlative confocal and super-resolution imaging. This enables colocalization and protein interaction studies at the nanometer scale.

  • Combined resonant galvanometer point scanning confocal and Nikon NSTORM Single molecule localization microscope capable of ~20nm resolution. 
  • Inverted Ti2 stand with 10, 20X dry, 10X LWD Water immersion, and 40X, 60X immersion Oil and 100X Silicone objectives. 
  • Motorized stage and software for automated tiling and stitching.
  • 6 laser lines: 405, 445, 488, 514, 561, and 647.
  • Princeton Instruments ProEM camera.

Applications

  • Single-Molecule Localization (STORM/PALM) achieves ~20–30 nm resolution and resolves structures beyond the diffraction limit. Ideal for nanoscale organization of proteins and complexes.
  •  Membrane & Surface Imaging (TIRF/STORM), facilitating high-contrast imaging at the cell membrane. Aids in the study of receptor dynamics, endocytosis/exocytosis, and/or cell adhesion complexes.
  • 3D Localization Microscopy: Axial (z-axis) resolution with specialized optics enabling 3D reconstruction of nanoscale structures.

Nikon W1 Spinning Disk

Nikon W1Nikon W1 spinning disk

  • High-speed spinning disk confocal on Nikon Ti2 inverted microscope, designed for rapid fluorescence imaging.
  • Provides enhanced signal-to-noise ratio, ultra-wide field of view, and improved light efficiency.
  • Together with the GATACA Live-SR unit, it provides super-resolution capability with a maximum resolution of 105nm. 
  • Enables gentle imaging with reduced phototoxicity and photobleaching, ideal for live samples.
  • Equipped with a stage-top incubation chamber for imaging live samples.
  • Motorized stage and software for automated tiling, stitching, and reconstruction
  • 7 laser lines for multicolor imaging (list them out)
  • Dual Hamamatsu sCMOS camera for simultaneous two-channel imaging.
  • Availability of two pinhole sizes (50um and 25um) to cover a wider range of objective magnifications. 
  • Equipped with Digital Micromirror Device (DMD)  for high-speed, patterned photo-stimulation, enabling precise optogenetics, photo-activation, and FRAP (Fluorescence Recovery After Photobleaching).
  • Availability of TIRF optics to enable high-contrast, surface-specific imaging of samples within 100-200 nm of the coverslip, minimizing background fluorescence. 
  • NIS-Elements General Analysis 3 (GA3) to create customized, automated imaging and quantification workflows.

Applications

  • Live-cell imaging of dynamic processes (cell division, migration, tracking)
  • Calcium signalling and other fast dynamic events. 
  • Large-area tile scans of sectioned tissue samples. 
  • Organoids, spheroids, embryos, and other thick 3D cell culture imaging.
  • Imaging of small model organisms (e.g., zebrafish, C. elegans).
  • Cell adhesion studies and other cellular dynamics occurring within ~100nm of the coverslip surface can be observed using TIRF optics.
  • Photoactivation/photoconversion, optogenetics, FRET, patterned stimulation, etc. 
  • High-content screening for automated, high-throughput testing and cellular studies.
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