Monoclonal antibodies (mAbs) are indispensable tools for the study, diagnosis and treatment of pathological conditions. The major purpose of the Epitope Recognition Immunoreagent Core (ERIC) is to assist RDCC investigators with the development, characterization and production of monoclonal reagents relevant to the study of rheumatic diseases (RDs). The ERIC has evolved from expansion and diversification of the Arthritis and Musculoskeletal Center's Hybridoma Core Facility which has been in operation since 1981. In addition to supplying traditional hybridoma services, the ERIC provides RDCC investigators with novel approaches for mAb development as well as expertise in immunoassay design, epitope characterization, and phage display technology. The core provides standard hybridoma services such as: procurement and housing of pathogen-free rodents, design and coupling of peptide immunogens, planning and implementation of immunization protocols, immunoassay design, sera testing, performance effusions and screening assays, single cell cloning, isotyping and large-scale production and purification of mAbs. At present, the core maintains a freezer inventory of approximately 10,000 vials which includes hybridomas produced in house and also commonly requested hybridoma lines obtained from American Type Tissue Collection (ATCC) or deposited by individual investigators. By virtue of the ERIC's 25 year association with UAB's Arthritis and Musculoskeletal Disease Center, many of hybridomas stored in the ERIC are related to the study of RDs. A panel of commonly requested monoclonal reagents is made available to RDCC investigators through the ERIC including; anti-tag mAbs (i.e. MYC, HA, HIS, GST, GFP, FLAG), anti-mouse and human CD mAbs and rat and mouse isotype-matched control mAbs. Another important function of the ERIC is to provide RDCC investigators with novel, state-of-the-art methodologies that are not readily available from other sources. Antibody phage display technology has been available through the core since 2000 and more recently peptide phage display was incorporated. Another specialized technology that is provided by the core is avian monoclonal antibody development. Avian mAb technology provides an alternative strategy for deriving high affinity mAbs to highly conserved mammalian proteins.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
2P30AR048311-06
Application #
7352456
Study Section
Special Emphasis Panel (ZAR1-KM-K (M1))
Project Start
2007-09-01
Project End
2012-08-31
Budget Start
2007-09-01
Budget End
2008-08-31
Support Year
6
Fiscal Year
2007
Total Cost
$82,650
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Yang, Zhengrong; Hildebrandt, Ellen; Jiang, Fan et al. (2018) Structural stability of purified human CFTR is systematically improved by mutations in nucleotide binding domain 1. Biochim Biophys Acta Biomembr 1860:1193-1204
Smith, Samuel R; Schaaf, Kaitlyn; Rajabalee, Nusrah et al. (2018) The phosphatase PPM1A controls monocyte-to-macrophage differentiation. Sci Rep 8:902
Chen, Wei; Zhu, Guochun; Jules, Joel et al. (2018) Monocyte-Specific Knockout of C/ebp? Results in Osteopetrosis Phenotype, Blocks Bone Loss in Ovariectomized Mice, and Reveals an Important Function of C/ebp? in Osteoclast Differentiation and Function. J Bone Miner Res 33:691-703
Wang, Yong; Schafer, Cara C; Hough, Kenneth P et al. (2018) Myeloid-Derived Suppressor Cells Impair B Cell Responses in Lung Cancer through IL-7 and STAT5. J Immunol 201:278-295
Jones, Robert B; Dorsett, Kaitlyn A; Hjelmeland, Anita B et al. (2018) The ST6Gal-I sialyltransferase protects tumor cells against hypoxia by enhancing HIF-1? signaling. J Biol Chem 293:5659-5667
Bandari, Shyam K; Purushothaman, Anurag; Ramani, Vishnu C et al. (2018) Chemotherapy induces secretion of exosomes loaded with heparanase that degrades extracellular matrix and impacts tumor and host cell behavior. Matrix Biol 65:104-118
Jo, SeongHo; Chen, Junqin; Xu, Guanlan et al. (2018) miR-204 Controls Glucagon-Like Peptide 1 Receptor Expression and Agonist Function. Diabetes 67:256-264
Stafman, Laura L; Williams, Adele P; Garner, Evan F et al. (2018) Targeting PIM Kinases Affects Maintenance of CD133 Tumor Cell Population in Hepatoblastoma. Transl Oncol 12:200-208
Hamilton, Jennie A; Wu, Qi; Yang, PingAr et al. (2018) Cutting Edge: Intracellular IFN-? and Distinct Type I IFN Expression Patterns in Circulating Systemic Lupus Erythematosus B Cells. J Immunol 201:2203-2208
Yang, Zhenhua; Shah, Kushani; Busby, Theodore et al. (2018) Hijacking a key chromatin modulator creates epigenetic vulnerability for MYC-driven cancer. J Clin Invest 128:3605-3618

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