The Integrated Microscopy Facility (IMF) functions as a supervised, user-based Core providing state-of-theart microscopy imaging capabilities to UCCRC members and other University investigators. The primary mission of the Facility is to provide a valuable, unique service to the University community by furnishing highquality microscopy instrumentation, image analysis tools, and expert assistance. In addition, maintaining equipment in optimal condition and training users require skilled technical personnel, something that individual laboratories typically cannot afford. Because imaging technology and computational capacity are evolving so rapidly, it is extremely difficult for individual researchers to maintain or afford cutting-edge capabilities. Integrated Microscopy offers one of the most flexible and informative tools available to researchers, offering scales of detail ranging from tens of millimeters to less than 10 nanometers with appropriate techniques, Available techniques provided by the IMF range from classic color histological stain imaging, to contrast generation in unstained cells, to fluorescence technologies. Fluorescence methods continue to offer the greatest range of applications ranging from localization of multiple targets to readout of biochemical or physiologic parameters in either fixed or living preparations. Accordingly, the greatest resources of the IMF are allocated to fluorescence microscopy. By merging the microscopy facilities created by several campus entities, the combined pool of resources is more efficiently managed and maintained, while also increasing access, capabilities, and capacity for UCCRC member research. Overall use of the IMF has increased close to three times the activity reported in the 2001 CCSG submission. Over 63 peer-reviewed investigators across six Scientific Programs routinely use the IMF, totaling 49% of Facility usage. Services provided by the IMF consist of the following: ? Provide state-of-the-art microscopy imaging capabilities including brightfield (color, DIG, etc), fluorescence (multi-dimension;TIRFM;bleaching, etc), high-resolution, -speed, -sensitivity, confocal, and physiologic techniques. ? Provide training on all instruments and expert advice to investigators regarding experiment design and execution. Provide oversight to assure proper equipment use and minimize breakage. ? Provide computers including networked data servers and software for image analysis and publication. ? Serve as an educational resource for University investigators in the use of current microscopy techniques and foster interactions among users.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014599-36
Application #
8244553
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2011-04-01
Budget End
2012-03-31
Support Year
36
Fiscal Year
2011
Total Cost
$113,763
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Hope, C Matthew; Webber, Jemma L; Tokamov, Sherzod A et al. (2018) Tuned polymerization of the transcription factor Yan limits off-DNA sequestration to confer context-specific repression. Elife 7:
Wu, Chengyue; Pineda, Federico; Hormuth 2nd, David A et al. (2018) Quantitative analysis of vascular properties derived from ultrafast DCE-MRI to discriminate malignant and benign breast tumors. Magn Reson Med :
Wong, Gabrielle S; Zhou, Jin; Liu, Jie Bin et al. (2018) Targeting wild-type KRAS-amplified gastroesophageal cancer through combined MEK and SHP2 inhibition. Nat Med 24:968-977
Ni, Kaiyuan; Lan, Guangxu; Chan, Christina et al. (2018) Nanoscale metal-organic frameworks enhance radiotherapy to potentiate checkpoint blockade immunotherapy. Nat Commun 9:2351
Meisel, Marlies; Hinterleitner, Reinhard; Pacis, Alain et al. (2018) Microbial signals drive pre-leukaemic myeloproliferation in a Tet2-deficient host. Nature 557:580-584
Webber, Jemma L; Zhang, Jie; Massey, Alex et al. (2018) Collaborative repressive action of the antagonistic ETS transcription factors Pointed and Yan fine-tunes gene expression to confer robustness in Drosophila. Development 145:
Wei, Jiangbo; Liu, Fange; Lu, Zhike et al. (2018) Differential m6A, m6Am, and m1A Demethylation Mediated by FTO in the Cell Nucleus and Cytoplasm. Mol Cell 71:973-985.e5
Boisclair Lachance, Jean-François; Webber, Jemma L; Hong, Lu et al. (2018) Cooperative recruitment of Yan via a high-affinity ETS supersite organizes repression to confer specificity and robustness to cardiac cell fate specification. Genes Dev 32:389-401
Szmulewitz, Russell Z; Peer, Cody J; Ibraheem, Abiola et al. (2018) Prospective International Randomized Phase II Study of Low-Dose Abiraterone With Food Versus Standard Dose Abiraterone In Castration-Resistant Prostate Cancer. J Clin Oncol 36:1389-1395
Kudron, Michelle M; Victorsen, Alec; Gevirtzman, Louis et al. (2018) The ModERN Resource: Genome-Wide Binding Profiles for Hundreds of Drosophila and Caenorhabditis elegans Transcription Factors. Genetics 208:937-949

Showing the most recent 10 out of 668 publications