The Hybridoma Core Facility will be used by approximately 30 UM-MAC investigators who are pursuing a variety of research projects that require monoclonal antibodies. The hybridoma Facility (HF) is a research laboratory, the purpose of which is to generate somatic-cell hybrids (hybridomas) that produce monoclonal antibodies of desired specificity. It is supported by the Michigan Diabetes Research and Training Center (MDRTC), and by the University of Michigan Multipurpose Arthritis Center (UM-MAC), for use by investigators within these centers, currently at a 10% recharge. It is also used by other investigators on a full recharge basis. Services include immunization of mice, fusion of B lymphocytes with myeloma cells to create hybridomas, subcloning and cryopreservation of hybridomas, antibody isotyping and production of ascites in mice. Consultation is available from the Hybridoma Core directors in design of immunization strategies and screening assays to ensure efficient detection of the desired monoclonal antibodies. The majority of hybridomas produced in the core are of murine origin, but rat, hamster and human hybridomas have also been produced. Since its establishment in 1980 the Hybridoma Facility has produced monoclonal antibodies against a wide variety of lymphocyte surface antigens, tumor cell antigens, purified proteins, hormones, hormone receptors and recombinant proteins. In the past four years of UM-MAC support (1993-1996) more than 65 fusions were performed for UM-MAC investigators. Subcloning was performed for more than 350 hybridomas and almost 400 monoclonal antibody batches were produced in murine ascites. A variety of specialized procedures have been added during the current funding cycle to address various needs of UM-MAC investigators. The current proposal will allow this facility to continue to provide up- to-date hybridoma technology for UM-MAC laboratories. The core will also provide collaborative and consultive services for the UM-MAC vector core in assisting investigators who may wish to select recombinant antibody- like reagents from phage display libraries. Through these initiatives, the Hybridoma Core will remain on the cutting edge of monoclonal antibody technology, and continue to provide optimal service to UM-MAC investigators.

Project Start
1998-01-15
Project End
1998-12-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
20
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Davis, Shannon W; Keisler, Jessica L; Pérez-Millán, María I et al. (2016) All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors. Endocrinology 157:1385-96
Gorelik, Gabriela; Sawalha, Amr H; Patel, Dipak et al. (2015) T cell PKC? kinase inactivation induces lupus-like autoimmunity in mice. Clin Immunol 158:193-203
Rillamas-Sun, Eileen; Harlow, Siobán D; Randolph Jr, John F (2014) Grandmothers' smoking in pregnancy and grandchildren's birth weight: comparisons by grandmother birth cohort. Matern Child Health J 18:1691-8
O'Leary, Erin E; Mazurkiewicz-Muñoz, Anna M; Argetsinger, Lawrence S et al. (2013) Identification of steroid-sensitive gene-1/Ccdc80 as a JAK2-binding protein. Mol Endocrinol 27:619-34
Sugg, Kristoffer B; Rosenthal, Andrew H; Ozaki, Wayne et al. (2013) Quantitative comparison of volume maintenance between inlay and onlay bone grafts in the craniofacial skeleton. Plast Reconstr Surg 131:1014-21
Perez-Millan, Maria Ines; Zeidler, Michael G; Saunders, Thomas L et al. (2013) Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes. Genesis 51:785-92
Fang, Qing; Giordimaina, Alicia M; Dolan, David F et al. (2012) Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment. J Assoc Res Otolaryngol 13:173-184
Tao, Jiayi; Zhu, Min; Wang, He et al. (2012) SEC23B is required for the maintenance of murine professional secretory tissues. Proc Natl Acad Sci U S A 109:E2001-9
Rillamas-Sun, Eileen; Sowers, MaryFran R; Harlow, Sioban D et al. (2012) The relationship of birth weight with longitudinal changes in body composition in adult women. Obesity (Silver Spring) 20:463-5
Zacharias, William J; Madison, Blair B; Kretovich, Katherine E et al. (2011) Hedgehog signaling controls homeostasis of adult intestinal smooth muscle. Dev Biol 355:152-62

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