? M&I CORE The Microscopy and Imaging Analysis (M&I) core is the major component of the vision research core at UCLA, with 18 research laboratories projecting moderate or extensive usage. The M&I core facilities have been revamped in terms of both new laboratories and new equipment. The core is now housed in dedicated core space that was completely renovated. Over the past two years, a new JEOL JEM 1400plus electron microscope, a new Deltavision OMX super resolution microscope, and a new Nikon spinning disk confocal microscope were purchased, and are now all up and running, providing users with state-of-the-art imaging. The M&I core is equipped with facilities and equipment for: 1) sample preparation, including the preservation of tissue to be studied in a fixed state, sectioning (from thick to ultrathin), and the preparation of live tissues for live-cell imaging; 2) many different forms of imaging capabilities, from light to super resolution to EM; 3) image analysis, with a software suite, including Imaris. Thus, together with technical support in all aspects, the core provides users facilities, assistance, and training in sample preparation, imaging and image acquisition, and image analysis. The M&I core thus facilitates basic and preclinical research supported by NIH/NEI on UCLA campus by providing access to facilities, equipment, and technical skills that cannot be found in individual laboratories.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Center Core Grants (P30)
Project #
2P30EY000331-53
Application #
10020827
Study Section
Special Emphasis Panel (ZEY1)
Project Start
1997-03-01
Project End
2025-06-30
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
53
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Glasgow, Ben J; Abduragimov, Adil R (2018) Interaction of ceramides and tear lipocalin. Biochim Biophys Acta Mol Cell Biol Lipids 1863:399-408
Demer, Joseph L (2018) Knobby Eye Syndrome. Strabismus 26:33-41
Glasgow, Ben J; Abduragimov, Adil R (2018) Ligand binding studies by high speed centrifugal precipitation and linear spectral summation using ultraviolet-visible absorption spectroscopy. MethodsX 5:345-351
Hazim, Roni A; Volland, Stefanie; Yen, Alice et al. (2018) Rapid differentiation of the human RPE cell line, ARPE-19, induced by nicotinamide. Exp Eye Res 179:18-24
Glasgow, Ben J; Abduragimov, Adil R (2018) Data on Orphan tear lipid analogs, synthesis and binding to tear lipocalin. Data Brief 18:999-1004
Sarria, Ignacio; Cao, Yan; Wang, Yuchen et al. (2018) LRIT1 Modulates Adaptive Changes in Synaptic Communication of Cone Photoreceptors. Cell Rep 22:3562-3573
Peng, Yingqian; Baulier, Edouard; Ke, Yifeng et al. (2018) Human embryonic stem cells extracellular vesicles and their effects on immortalized human retinal Müller cells. PLoS One 13:e0194004
Clark, Robert A; Demer, Joseph L (2018) The Globe's Eccentric Rotational Axis: Why Medial Rectus Surgery Is More Potent than Lateral Rectus Surgery. Ophthalmology 125:1234-1238
Van Eps, Ned; Altenbach, Christian; Caro, Lydia N et al. (2018) Gi- and Gs-coupled GPCRs show different modes of G-protein binding. Proc Natl Acad Sci U S A 115:2383-2388
Shin, Andrew; Park, Joseph; Demer, Joseph L (2018) Opto-mechanical characterization of sclera by polarization sensitive optical coherence tomography. J Biomech 72:173-179

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