https://medicine.ouhsc.edu/academic-departments Parent Page: Academic Departments id: 36729 Active Page: Super-Resolution Imaging Core (SRIC) id: 36731 Portal ID: 248

Super-Resolution Imaging Core (SRIC)

The Super-Resolution Imaging Core (SRIC) at the University of Oklahoma Health Campus is the first facility of its kind in Oklahoma, providing investigators with access to advanced super-resolution imaging technologies, expert microscopy support, and quantitative image analysis services. The core integrates established Nikon N-SIM E/STORM and Nikon CSU-W1/SoRa super-resolution microscopes with a new Lattice LightSheet microscope, the only instrument in the state capable of super-resolution live-cell imaging. Together, these platforms enable visualization of subcellular structures and dynamic cellular processes with exceptional spatial and temporal resolution in both fixed and living specimens. Located within the Biomedical Sciences Building, the SRIC is staffed by experienced imaging scientists who provide consultation, training, experimental design support, and image analysis expertise. By combining state-of-the-art instrumentation, dedicated personnel, and computational resources, the SRIC supports a broad range of biomedical research applications and facilitates discoveries in sensory biology, physiology, and cellular function.

FEATURED INSTRUMENTATION

Super-resolution Nikon N-SIM E/STORM microscope

Nikon N-SIM E/STORM Microscope

The microscope is built on a Nikon Ti2 inverted fluorescence microscope equipped for Differential Interference Contrast and fluorescence imaging in the blue, green, red, and far red channels at magnifications of 4X, 10X, 20X, and 100X.

  • Super-resolution imaging modalities: TIRF, Structured Illumination Microscopy (SIM), and Stochastic Optical Reconstruction Microscopy (STORM)
  • Stage top incubator for live cell imaging
  • Nikon Elements software for image acquisition and analysis
  • User fee: $20/hr

Super-resolution Nikon CSU-W1/SoRa spinning disk confocal microscope

Nikon CSU-W1/SoRa Spinning Disk Confocal Microscope

The microscope is built on a Nikon Ti2 inverted fluorescence microscope equipped for Differential Interference Contrast and fluorescence imaging in the blue, green, red, and far red channels at magnifications of 4X, 10X, 20X, 40X, 60X, and 100X.

  • SoRa attachment enables super-resolution imaging
  • Spinning disk design permits confocal imaging through specimens up to 200-300 micrometers thick
  • Stage top incubator for live cell imaging
  • Fast galvo scanner for dynamic imaging methods including FRAP, photoconversion, and photostimulation
  • User fee: $20/hr

Super-resolution Nikon Ti2 AX-R/NSPARC-FLIM/widefield Fluorescence Live- Cell Imaging Microscope

Nikon Ti2 AX-R/NSPARC FLIM Live Cell Imaging Microscope

This multi-functional microscope is built on a Nikon Ti2 inverted fluorescence microscope equipped with two independent illumination decks for high-speed super-resolution and widefield imaging.

  • First deck configured for high-speed super-resolution imaging using Nikon AX-R/NSPARC confocal imaging
  • Supports Fluorescence Lifetime Imaging (FLIM) via PicoQuant software and hardware for Time-Correlated Single Photon Counting
  • Enables local environment sensing and detection of molecular interactions via FLIM/FRET
  • Stage-mounted live-cell imaging chambers for confocal, FLIM, or widefield imaging modes
  • Nikon Elements software for image acquisition and PicoQuant software for FLIM analyses

Lattice LightSheet super-resolution system

This system combines gentle light sheet imaging and fast image acquisitions to enable dynamic imaging of full sample volumes at subcellular resolutions. The lattice-structured light sheet greatly reduces photobleaching and phototoxicity, providing unsurpassed imaging of living specimens for hours to days. This system includes a Lattice LightSheet microscope utilizing Bessel beam lattice sheet illumination via cylindrical lenses and high-speed SLM for multicolor imaging, annular mask array for various lightsheets, galvo mirrors to control lattice movement in x and z, cameras in image space to inspect the lattice pattern, 25x/1.1NA water immersion detection objective, 28x/0.71NA water immersion illumination objective, x,y translation stages and piezo imaging objective control.

SRIC DIRECTORS

Elise O'Connell

Jody Summers, PhD

SRIC Administrative Director
 
DMEI Basement Room 29 608Stanton L.Young Blvd
Oklahoma City, Ok 73104
Luciana Medeiros

Dr.Yiyang Gong, PhD

SRIC Imaging Scientific Co-Director Lattice
LightSheet Imaging Specialist
 
940 Stanton L. Young Blvd. BMSB 553A
Oklahomacity, ok 73104
Andrés Henao-Martínez

Dr.Tomoharu Kanie, PhD

SRIC Imaging Scientific Co-Director Lattice
LightSheet Imaging Specialist
 
940 Stanton L. Young Blvd. BMSB 111
Oklahomacity, ok 73104

Contact Us

Department of Cell Biology

Sean Netterville | Admin Coordinator
940 Stanton L. Young Blvd., BMSB 553
Oklahoma City, OK 73104

(405) 271-2377
BSAdmin@ouhsc.edu
Fax: (405) 271-3548