A large number of investigators at the University of Massachusetts Medical School who perform diabetes-related research require cell culture and associated techniques. The Cell Science Core provides services in four major areas: 1) Operation of a supply center where investigators can order supplies at a significant discount for next day delivery. 2) Cryopreservation of tissue and cell stocks and centralized storage of cell lines including a DERC cell bank. 3) Provision of specialized immune cell culture services including a) spleen harvesting and cell fusion for the production of hybridomas and monoclonal antibodies (mAbs), b) purification of mAbs and c) production of large quantities of mAbs using CellMax cartridges. 4) Provisison of wide variety of routine cell culture services. These include cell cloning, routine maintenance and production of cell lines in monolayer and suspension culture, specialized media preparation, primary culture, mycoplasma testing, and the provision of unique diabetes-related reagents such as insulin-expressing cell lines. The Core has a documented track record of high quality service to the DERC community and recently relocated to excellent laboratory space in the school's new Biotech I building, which is close to all of the research laboratories on the Univeristy campus. Facilities include separate rooms for cell and tissue culture, cell storage, and supply center storage. The laboratories are equipped with two laminar flow hoods and nine CO2 incubators (five recently provided by the University), a programmed cell freezer, liquid nitrogen cell storage tanks, centrifuges, microscopes, and all equipment needed to prepare liquid culture media and monoclonal antibodies. In brief, the Cell Science Core enhances the productivity of diabetes researchers by providing services not available to individual laboratories, serving as a supply center, and providing advice and expertise on hybridoma and monoclonal antibody production-all at costs much lower than those that would be borne by investigators without access to the Facility.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK032520-23
Application #
7311471
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
23
Fiscal Year
2006
Total Cost
$99,010
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Desai, Paurav B; San Agustin, Jovenal T; Stuck, Michael W et al. (2018) Ift25 is not a cystic kidney disease gene but is required for early steps of kidney development. Mech Dev 151:10-17
Ly, Socheata; Navaroli, Deanna M; Didiot, Marie-Cécile et al. (2017) Visualization of self-delivering hydrophobically modified siRNA cellular internalization. Nucleic Acids Res 45:15-25
Wang, Feng; McCannell, Kurtis N; Boškovi?, Ana et al. (2017) Rlim-Dependent and -Independent Pathways for X Chromosome Inactivation in Female ESCs. Cell Rep 21:3691-3699
Watkin, Levi B; Mishra, Rabinarayan; Gil, Anna et al. (2017) Unique influenza A cross-reactive memory CD8 T-cell receptor repertoire has a potential to protect against EBV seroconversion. J Allergy Clin Immunol 140:1206-1210
LeBlanc, Scott E; Wu, Qiong; Lamba, Pallavi et al. (2016) Promoter-enhancer looping at the PPAR?2 locus during adipogenic differentiation requires the Prmt5 methyltransferase. Nucleic Acids Res 44:5133-47
Wang, Feng; Shin, JongDae; Shea, Jeremy M et al. (2016) Regulation of X-linked gene expression during early mouse development by Rlim. Elife 5:
Kincaid, Eleanor Z; Murata, Shigeo; Tanaka, Keiji et al. (2016) Specialized proteasome subunits have an essential role in the thymic selection of CD8(+) T cells. Nat Immunol 17:938-45
Townsley, E; O'Connor, G; Cosgrove, C et al. (2016) Interaction of a dengue virus NS1-derived peptide with the inhibitory receptor KIR3DL1 on natural killer cells. Clin Exp Immunol 183:419-30
Wyss, Lena; Stadinski, Brian D; King, Carolyn G et al. (2016) Affinity for self antigen selects Treg cells with distinct functional properties. Nat Immunol 17:1093-101
Delong, Thomas; Wiles, Timothy A; Baker, Rocky L et al. (2016) Pathogenic CD4 T cells in type 1 diabetes recognize epitopes formed by peptide fusion. Science 351:711-4

Showing the most recent 10 out of 707 publications