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    High Resolution Imaging Facility at UAB
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    High Resolution Imaging Facility at UAB

Mission Statement

The High Resolution Imaging Facility (HRIF) provides state-of-the-art imaging resources and technical support to the UAB community. HRIF offers electron microscopy and light microscopy including confocal, live cell, multi-photon, widefield, super resolution, and image analysis. To effectively implement these technologies, we provide consultations, expert training, and support for all our systems. We are open to all UAB investigators as well as other investigators in the research community.

 

HRIF News & Events

 

  • ONI Lunch & Learn: Breaking through resolution barriers

    Hosted by UAB High Resolution Imaging Facility (HRIF)
    Monday, December 2, 2024 12:00 PM CST
    Shelby Biomedical Research Building Rm. 105

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  • Sub-micron IR/Raman/Fluorescence Workshop

    Hosted by Photothermal Spectroscopy Corp
    Wednesday, October 16, 2024 12:00PM – 2:00PM
  • Data Management Notice for IRCP Cores

    Please read important information regarding data management, specifically noting that IRCP cores are not responsible for data storage after services have been rendered. A formal policy document will be posted soon. Please have attached flyer image as well.
  • 4 cutting-edge machines powering UAB discoveries


    Photo by ANDREA MABRY | University Relations

    Alexa Mattheyses, Ph.D. (right), director of the UAB High-Resolution Imaging Facility, and Robert Grabski, Ph.D., research associate in the High-Resolution Imaging Facility. They are pictured with the Zeiss Lightsheet 7 light sheet microscope, an advanced imaging device capable of fluorescent imaging of living cells and tissues.

    What it does: A light sheet fluorescent microscope, or LSFM, allows researchers to visualize the relationships between cells and proteins in intact tissues, organs and organisms at high volume and at a range of sizes and resolutions. Because of its image acquisition speed, the Zeiss Lightsheet 7 can perform data collection from large samples rapidly and efficiently, “allowing us to image far larger samples than we are currently capable of, including whole organisms and intact cleared tissues,” Mattheyses wrote in her grant abstract. Light sheet fluorescent microscopy also “substantially reduces photobleaching and photodamage,” she added. Samples do not need to be mounted on a slide or coverslip, “allowing more physiological imaging of model organisms and intact tissues,” Mattheyses said. “Finally, samples can be rotated relative to the imaging plane, allowing ideal orientation and collection of multiple views.”

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  • Zeiss Lightsheet 7 is here!

    We are very excited to announce that our Zeiss Lightsheet7 microscope, purchased with support of a NIH S10 grant, is fully operational! This microscope brings unique imaging capabilities previously unavailable to UAB research community, The Zeiss Lightsheet 7 Fluorescent Microscope (LSFM) is ideal for fast and gentle imaging of whole living model organisms (zebrafish, organoids, tadpole embryo, various tissues) as they develop over extended periods of time and imaging of large optically cleared specimens with subcellular resolution. Dedicated optics, sample chambers and holders allow adaption to the refractive index of your chosen clearing method.

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