The goal for the DNA Sequencing Shared Resource is to provide high quality DNA sequence analysis at low cost and with rapid turn-around to members of the Cancer Center. The facility operates ABI 373 and 377 automated DNA sequencers, an ABI Catalyst 800 Robotic Work Station, an ABI DNA/RNA synthesizer, and six support computers with appropriate software. Funds are requested to support a portion of salaries of four individuals involved in facility operations and 15 percent of the service contracts for the various apparatus in the facility. The use of the DNA Sequence Facility has increased over 500 percent since the time of the last review. Usage is primarily measured in terms of DNA sequence output, expressed as number of base pairs. The number of investigators that have used the DNA Sequencing Share Resource is a second measure of utilization. Approximately 1.2 million base pairs of sequence were generated in the 1995/1996 fiscal year. Twenty-five Cancer Center members, including 23 with peer-reviewed funded projects, used the facility on 26 funded projects; 52 non-members used it as well. The relative use by members of the Cancer Center, expressed as percentage of bases sequenced, was 44 percent. The total capacity of the shared resource was not provided in the written materials, but at the site visit, it was indicated that the use of the resource had increased further and that it is currently operating at 80 percent of capacity. The applicants anticipate a continued increase in use of the facility. The Howard Hughes Medical Institute at UCLA contributed the ABI 377 automated DNA sequencer to the Shared Resource output.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016042-28
Application #
6563718
Study Section
Project Start
2001-12-01
Project End
2002-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
28
Fiscal Year
2002
Total Cost
$167,178
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Glenn, Beth A; Hamilton, Ann S; Nonzee, Narissa J et al. (2018) Obesity, physical activity, and dietary behaviors in an ethnically-diverse sample of cancer survivors with early onset disease. J Psychosoc Oncol 36:418-436
Tsai, Wen-Ting K; Wu, Anna M (2018) Aligning physics and physiology: Engineering antibodies for radionuclide delivery. J Labelled Comp Radiopharm 61:693-714
Lisova, Ksenia; Sergeev, Maxim; Evans-Axelsson, Susan et al. (2018) Microscale radiosynthesis, preclinical imaging and dosimetry study of [18F]AMBF3-TATE: A potential PET tracer for clinical imaging of somatostatin receptors. Nucl Med Biol 61:36-44
Chang, Yu-Ling; Rossetti, Maura; Vlamakis, Hera et al. (2018) A screen of Crohn's disease-associated microbial metabolites identifies ascorbate as a novel metabolic inhibitor of activated human T cells. Mucosal Immunol :
Kiertscher, Sylvia M; Gangalum, Pallavi R; Ibrahim, Grace et al. (2018) A Prospective Study of Humoral and Cellular Immune Responses to Hepatitis B Vaccination in Habitual Marijuana Smokers. J Neuroimmune Pharmacol 13:219-229
Jia, Qingmei; Bowen, Richard; Dillon, Barbara Jane et al. (2018) Single vector platform vaccine protects against lethal respiratory challenge with Tier 1 select agents of anthrax, plague, and tularemia. Sci Rep 8:7009
Van, Christina; Condro, Michael C; Lov, Kenny et al. (2018) PACAP/PAC1 Regulation of Inflammation via Catecholaminergic Neurons in a Model of Multiple Sclerosis. J Mol Neurosci :
Leoh, Lai Sum; Kim, Yoon Kyung; Candelaria, Pierre V et al. (2018) Efficacy and Mechanism of Antitumor Activity of an Antibody Targeting Transferrin Receptor 1 in Mouse Models of Human Multiple Myeloma. J Immunol 200:3485-3494
Hicks, Michael R; Hiserodt, Julia; Paras, Katrina et al. (2018) ERBB3 and NGFR mark a distinct skeletal muscle progenitor cell in human development and hPSCs. Nat Cell Biol 20:46-57
Tsang, Eric J; Wu, Benjamin; Zuk, Patricia (2018) MAPK signaling has stage-dependent osteogenic effects on human adipose-derived stem cells in vitro. Connect Tissue Res 59:129-146

Showing the most recent 10 out of 767 publications