The Molecular Recognition Core Facility consists of two parts. One part contains equipment and space that was a part of the previous """"""""Molecular Biology Core Facility """""""" and continues to be extensively utilized by Center investigators in their projects. The overall goal is to provide needed equipment and services in a cost-effective manner. The other component is a joint facility designed to provide new, essential high-throughput services related to the general area of molecular recognition to both Center and University investigators. The goal of the Molecular Recognition Core Facility is to provide investigators with reagents and equipment for the production, detection, and characterization of biomolecules. The facility is composed of three """"""""Resources,"""""""" the Antibody Resource, the Protein Expression Resource, and the BIAcore Resource. Each Resource provides unique, cost-effective services and expertise for Center and other University investigators. The goal of the Antibody Resource is to provide the expertise, reagents, and equipment for the production, detection, characterization, purification, and labeling of monoclonal and recombinant phage-displayed or soluble ScFv antibodies for research, diagnostic, or therapeutic use. Assays incorporating antibodies can also be developed to detect and/or quantify proteins, carbohydrates, or nucleic acids that occur as components of a biological or chemical milieu. The objective of the Antibody Resource is to provide hybridoma monoclonal and phage-displayed recombinant antibodies and antibody-based assays to Center investigators and other individuals throughout the University on a timely and cost-effective basis. The goal of the Antibody Resource is to provide the expertise, reagents, and equipment for the production, detection, characterization, purification, and labeling of monoclonal and recombinant phage-displayed or soluble ScFv antibodies for research, diagnostic, or therapeutic use. Assays incorporating antibodies can also be developed to detect and/or quantify proteins, carbohydrates, or nucleic acids that occur as components of a biological or chemical milieu. The objective of the Antibody Resource is to provide hybridoma monoclonal and phage-displayed recombinant antibodies and antibody-based assays to Center investigators and other individuals throughout the University on a timely and cost-effective basis. The goal of the Protein Expression Resource is to provide Center and other University investigators with reagents and equipment for large-scale protein production using the baculovirus expression system. Additionally, the Protein Expression Resource also provides investigators with equipment necessary to harvest large amounts of cellular material. The goal and the objective of the BIAcore Resource is to provide Center and other University investigators with access to the BIAcore 2000, an instrument from BIAcore Inc., that performs real-time biomolecular interaction analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES000267-42
Application #
7599206
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
Project End
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
42
Fiscal Year
2008
Total Cost
$170,130
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Wages, Phillip A; Kim, Hye-Young H; Korade, Zeljka et al. (2018) Identification and characterization of prescription drugs that change levels of 7-dehydrocholesterol and desmosterol. J Lipid Res 59:1916-1926
Neely, M Diana; Davison, Carrie Ann; Aschner, Michael et al. (2017) From the Cover: Manganese and Rotenone-Induced Oxidative Stress Signatures Differ in iPSC-Derived Human Dopamine Neurons. Toxicol Sci 159:366-379
Sha, Yan; Minko, Irina G; Malik, Chanchal K et al. (2017) Error-prone replication bypass of the imidazole ring-opened formamidopyrimidine deoxyguanosine adduct. Environ Mol Mutagen 58:182-189
Sugitani, Norie; Voehler, Markus W; Roh, Michelle S et al. (2017) Analysis of DNA binding by human factor xeroderma pigmentosum complementation group A (XPA) provides insight into its interactions with nucleotide excision repair substrates. J Biol Chem 292:16847-16857
Minko, Irina G; Rizzo, Carmelo J; Lloyd, R Stephen (2017) Mutagenic potential of nitrogen mustard-induced formamidopyrimidine DNA adduct: Contribution of the non-canonical ?-anomer. J Biol Chem 292:18790-18799
Rivara, Matthew B; Yeung, Catherine K; Robinson-Cohen, Cassianne et al. (2017) Effect of Coenzyme Q10 on Biomarkers of Oxidative Stress and Cardiac Function in Hemodialysis Patients: The CoQ10 Biomarker Trial. Am J Kidney Dis 69:389-399
Yan, H P; Roberts, L J; Davies, S S et al. (2017) Isolevuglandins as a gauge of lipid peroxidation in human tumors. Free Radic Biol Med 106:62-68
Deger, Serpil Muge; Hung, Adriana M; Ellis, Charles D et al. (2016) High Dose Omega-3 Fatty Acid Administration and Skeletal Muscle Protein Turnover in Maintenance Hemodialysis Patients. Clin J Am Soc Nephrol 11:1227-35
King-Morris, Kelli R; Deger, Serpil Muge; Hung, Adriana M et al. (2016) Measurement and Correlation of Indices of Insulin Resistance in Patients on Peritoneal Dialysis. Perit Dial Int 36:433-41
Lin, Ying-Chih; Owen, Nichole; Minko, Irina G et al. (2016) DNA polymerase ? limits chromosomal damage and promotes cell survival following aflatoxin exposure. Proc Natl Acad Sci U S A 113:13774-13779

Showing the most recent 10 out of 712 publications