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 #
5P30CA014599-27
Application #
6397815
Study Section
Project Start
2000-08-01
Project End
2002-03-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
27
Fiscal Year
2000
Total Cost
$289,716
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Trujillo, Jonathan A; Sweis, Randy F; Bao, Riyue et al. (2018) T Cell-Inflamed versus Non-T Cell-Inflamed Tumors: A Conceptual Framework for Cancer Immunotherapy Drug Development and Combination Therapy Selection. Cancer Immunol Res 6:990-1000
Zeng, Zongyue; Huang, Bo; Huang, Shifeng et al. (2018) The development of a sensitive fluorescent protein-based transcript reporter for high throughput screening of negative modulators of lncRNAs. Genes Dis 5:62-74
Lee, Ji-Hye; Park, Beom Seok; Han, Kang R et al. (2018) Insight Into the Interaction Between RNA Polymerase and VPg for Murine Norovirus Replication. Front Microbiol 9:1466
Cheng, Jason X; Chen, Li; Li, Yuan et al. (2018) RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia. Nat Commun 9:1163
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

Showing the most recent 10 out of 668 publications