) The VCC Flow Cytometry Shared Resource provides state-of-the-art analytical flow cytometry capabilities to Cancer Center researchers. It features a Coulter EPICS XL four-color analytical flow cytometer equipped with an automated carousel loader, and two computer workstations for data acquisition and analysis. In its current configuration, the flow cytometer is capable of simultaneously collecting data from up to eleven different parameters in parallel. The facility has trained staff and expert scientists who can provide guidance with experimental design, development and application of new techniques or reagents, and help in interpreting and analyzing data. The facility is directed by Dr. James Koh and has one staff person, Mr. Scott Tighe. Two-tiered services are available, including either 1) operator-assisted runs or 2) unassisted runs for researchers or their designees who have had appropriate training from facility staff. This is a new VCC-run facility that was established and run in 1999 because of an expressed need by VCC researchers, particularly in support of groups studying cancer-related growth control, apoptosis, and cell-cycle regulation. An independent institutional FACS core offering sorting capabilities is available to VCC researchers but we do not propose it for CCSG support. This is the first request for CCSG support for a VCC Flow Cytometry.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA022435-18
Application #
6457148
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
1978-08-01
Project End
2005-11-30
Budget Start
Budget End
Support Year
18
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Vermont & St Agric College
Department
Type
DUNS #
066811191
City
Burlington
State
VT
Country
United States
Zip Code
05405
Kelemen, Linda E; Abbott, Sarah; Qin, Bo et al. (2017) Cigarette smoking and the association with serous ovarian cancer in African American women: African American Cancer Epidemiology Study (AACES). Cancer Causes Control 28:699-708
Long, Patrick M; Tighe, Scott W; Driscoll, Heather E et al. (2015) Acetate supplementation as a means of inducing glioblastoma stem-like cell growth arrest. J Cell Physiol 230:1929-43
Tsen, Andrew R; Long, Patrick M; Driscoll, Heather E et al. (2014) Triacetin-based acetate supplementation as a chemotherapeutic adjuvant therapy in glioma. Int J Cancer 134:1300-10
Wagner, Darcy E; Bonenfant, Nicholas R; Parsons, Charles S et al. (2014) Comparative decellularization and recellularization of normal versus emphysematous human lungs. Biomaterials 35:3281-97
Long, Patrick M; Tighe, Scott W; Driscoll, Heather E et al. (2013) Acetate supplementation induces growth arrest of NG2/PDGFR?-positive oligodendroglioma-derived tumor-initiating cells. PLoS One 8:e80714
Sokocevic, Dino; Bonenfant, Nicholas R; Wagner, Darcy E et al. (2013) The effect of age and emphysematous and fibrotic injury on the re-cellularization of de-cellularized lungs. Biomaterials 34:3256-69
Long, Patrick M; Moffett, John R; Namboodiri, Aryan M A et al. (2013) N-acetylaspartate (NAA) and N-acetylaspartylglutamate (NAAG) promote growth and inhibit differentiation of glioma stem-like cells. J Biol Chem 288:26188-200
Bonenfant, Nicholas R; Sokocevic, Dino; Wagner, Darcy E et al. (2013) The effects of storage and sterilization on de-cellularized and re-cellularized whole lung. Biomaterials 34:3231-45
Murray, Janet M; Messier, Terri; Rivers, Jami et al. (2012) VDJ recombinase-mediated TCR ? locus gene usage and coding joint processing in peripheral T cells during perinatal and pediatric development. J Immunol 189:2356-64
Wallis, John M; Borg, Zachary D; Daly, Amanda B et al. (2012) Comparative assessment of detergent-based protocols for mouse lung de-cellularization and re-cellularization. Tissue Eng Part C Methods 18:420-32

Showing the most recent 10 out of 219 publications