CONFOCAL MICROSCOPY SHARED RESOURCE David McClay, Ph.D., Richard Fehon, Ph.D., Co-Directors The Confocal Microscopy Shared Resource provides a state-of-the-art Facility for obtaining images of cells in which single molecules are tagged with fluorescent markers. By confocal microscopy and computation methods, 3-D images resolve the spatial location of any tagged molecule in cells, tissues or organisms. The Facility provides training for use of the microscope and the microscope plus computational components are maintained and frequently upgraded. The Confocal Microscopy Shared Resource supports more than 47 laboratories in the Cancer Center. In recent years the Facility has been booked for more than 98% of available time and used by more than 100 different investigators per year. The output of papers that include confocal instrumentation is high. Over the past five years more than 80 papers plus 10 journal covers come from facility usage. This proposal provides a list of upgrades and eventual replacement of the Zeiss 410 instrument that constitutes the Facility. There will be a continuation of policies that kept the instrument on line for all but 4 days in 2003. This will maximize availability of the instrument. Fee charges will be kept at the minimum necessary to keep the instrument in operation at a high efficiency. Policies for maintaining the instrument as a high quality and effective tool for obtaining confocal images will be continued. A new instrument will be purchased in about two years in order to provide the community with a state-of-the-art facility.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA014236-35
Application #
7764703
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2009-01-01
Budget End
2009-12-31
Support Year
35
Fiscal Year
2009
Total Cost
$31,055
Indirect Cost
Name
Duke University
Department
Type
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Káradóttir, Ragnhildur T; Kuo, Chay T (2018) Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis. Annu Rev Neurosci 41:139-161
Han, Peng; Liu, Hongliang; Shi, Qiong et al. (2018) Associations between expression levels of nucleotide excision repair proteins in lymphoblastoid cells and risk of squamous cell carcinoma of the head and neck. Mol Carcinog 57:784-793
Xu, Yinghui; Wang, Yanru; Liu, Hongliang et al. (2018) Genetic variants in the metzincin metallopeptidase family genes predict melanoma survival. Mol Carcinog 57:22-31
Abdi, Khadar; Kuo, Chay T (2018) Laminating the mammalian cortex during development: cell polarity protein function and Hippo signaling. Genes Dev 32:740-741
Lu, Min; Sanderson, Sydney M; Zessin, Amelia et al. (2018) Exercise inhibits tumor growth and central carbon metabolism in patient-derived xenograft models of colorectal cancer. Cancer Metab 6:14
Qian, Danwen; Liu, Hongliang; Wang, Xiaomeng et al. (2018) Potentially functional genetic variants in the complement-related immunity gene-set are associated with non-small cell lung cancer survival. Int J Cancer :
Ashcraft, Kathleen A; Choudhury, Kingshuk Roy; Birer, Sam R et al. (2018) Application of a Novel Murine Ear Vein Model to Evaluate the Effects of a Vascular Radioprotectant on Radiation-Induced Vascular Permeability and Leukocyte Adhesion. Radiat Res 190:12-21
Ong, Cecilia T; Campbell, Brittany M; Thomas, Samantha M et al. (2018) Metaplastic Breast Cancer Treatment and Outcomes in 2500 Patients: A Retrospective Analysis of a National Oncology Database. Ann Surg Oncol 25:2249-2260
Duan, Bensong; Hu, Jiangfeng; Liu, Hongliang et al. (2018) Genetic variants in the platelet-derived growth factor subunit B gene associated with pancreatic cancer risk. Int J Cancer 142:1322-1331
Wu, Mengxi; Huang, Po-Hsun; Zhang, Rui et al. (2018) Circulating Tumor Cell Phenotyping via High-Throughput Acoustic Separation. Small 14:e1801131

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