The Fitch Monoclonal Antibody Facility is a shared resource with two major goals: (1) to provide investigators in the University of Chicago Cancer Research Center and other University of Chicago investigators with a highly accessible and economical means for developing high-quality monoclonal and polyclonal antibodies for the purposes of clinical or basic research using proven methodologies; (2) in addition we also work closely with the investigators to develop novel approaches for generating quality monoclonal antibodies that will be useful reagents in diagnosis and therapy. The facility presently provides investigators with guidance and technical expertise in developing reagents that are well suited to their specific research needs. We also provide services designed to augment the usefulness of reagents developed here or elsewhere, including hybridoma subcloning, monoclonal antibody isotyping or quantitation, ascites production or other methods of generating moderate levels of antibody for research proposes. We are collaborating with the Animal Resources Center in the development of efficient in vitro methods of antibody production. Monoclonal antibodies have become essential tools in the interdisciplinary approaches to biological research, and the variety of applications requiring monoclonal antibodies have continued to expand as this technology has developed. Monoclonal antibodies remain very powerful tool for immunophenotyping cells in the study of cancer, transplantation, and immunology. There usefulness has been extended in the biochemical analysis of normal and abnormal functions of these and other cells. Furthermore, monoclonal antibodies are pivotal elements in many experimental and clinical strategies for the diagnosis and treatment of certain diseases. Our ability to derive and produce monoclonal antibodies provides a highly accessible resource which meets a growing demand for such reagents in the Cancer Center research community.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA014599-26S1
Application #
6396722
Study Section
Project Start
1999-08-01
Project End
2000-07-31
Budget Start
Budget End
Support Year
26
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Johnson, Marianna B; Hoffmann, Joscelyn N; You, Hannah M et al. (2018) Psychosocial Stress Exposure Disrupts Mammary Gland Development. J Mammary Gland Biol Neoplasia 23:59-73
Sweis, Randy F; Zha, Yuanyuan; Pass, Lomax et al. (2018) Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer. J Immunother Cancer 6:24
Kathayat, Rahul S; Cao, Yang; Elvira, Pablo D et al. (2018) Active and dynamic mitochondrial S-depalmitoylation revealed by targeted fluorescent probes. Nat Commun 9:334
Liu, Jun; Eckert, Mark A; Harada, Bryan T et al. (2018) m6A mRNA methylation regulates AKT activity to promote the proliferation and tumorigenicity of endometrial cancer. Nat Cell Biol 20:1074-1083
Bhanvadia, Raj R; VanOpstall, Calvin; Brechka, Hannah et al. (2018) MEIS1 and MEIS2 Expression and Prostate Cancer Progression: A Role For HOXB13 Binding Partners in Metastatic Disease. Clin Cancer Res 24:3668-3680
Wood, Kevin; Byron, Elizabeth; Janisch, Linda et al. (2018) Capecitabine and Celecoxib as a Promising Therapy for Thymic Neoplasms. Am J Clin Oncol 41:963-966
Sample, Ashley; Zhao, Baozhong; Wu, Chunli et al. (2018) The Autophagy Receptor Adaptor p62 is Up-regulated by UVA Radiation in Melanocytes and in Melanoma Cells. Photochem Photobiol 94:432-437
Hrusch, C L; Manns, S T; Bryazka, D et al. (2018) ICOS protects against mortality from acute lung injury through activation of IL-5+ ILC2s. Mucosal Immunol 11:61-70
Hope, C Matthew; Webber, Jemma L; Tokamov, Sherzod A et al. (2018) Tuned polymerization of the transcription factor Yan limits off-DNA sequestration to confer context-specific repression. Elife 7:
Wong, Gabrielle S; Zhou, Jin; Liu, Jie Bin et al. (2018) Targeting wild-type KRAS-amplified gastroesophageal cancer through combined MEK and SHP2 inhibition. Nat Med 24:968-977

Showing the most recent 10 out of 668 publications