FACSymphony S6 Cell Sorter for Improving Basic, Clinical, and Translational Cancer Research Capabilities
FACSymphony S6 细胞分选仪可提高基础、临床和转化癌症研究能力
基本信息
- 批准号:10427630
- 负责人:
- 金额:$ 59.98万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-08-01 至 2024-07-31
- 项目状态:已结题
- 来源:
- 关键词:13 year oldAgeAnimal ExperimentsBiomedical ResearchCaliforniaCancer CenterCell Culture TechniquesCell SeparationCellsChargeClinicalColorCommunitiesContract ServicesCore FacilityEnsureFlow CytometryFlow Cytometry Shared ResourceFundingHourHumanImpairmentLasersLeadershipMissionModernizationNCI Center for Cancer ResearchPopulationResearchResearch PersonnelSafetySamplingSideSorting - Cell MovementSpeedTechnologyTrainingTraining and EducationUniversitiesVisionanticancer researchbasecost efficientfaculty researchimprovedinstrumentinstrumentationmeetingsprogramstranslational cancer research
项目摘要
PROJECT SUMMARY/ABSTRACT
The Flow Cytometry Shared Resource (FCSR) is a comprehensive core facility that has been an integral
component of the Moores Cancer Center (MCC) at the University of California, San Diego (UCSD) since 1990.
It serves all MCC research programs and the La Jolla biomedical research community at large with ready access
to high-speed flow cytometry-based analysis and cell sorting of dissociated cell populations from clinical
samples, animal experiments, and cell culture studies. The FCSR has been a highly utilized and essential core
facility critical to diverse research programs in the MCC. Between 2013-2018, the FCSR served 59 MCC
investigators and was utilized for nearly 4000 hours by MCC investigators. However, recent advances in FACS
technology have rendered current sorters in the FCSR mostly obsolete and incapable of meeting state-of-the-
art research needs, which threatens to limit critical advances in cancer research. The two cell sorters located in
the FCSR, a BD FACSAria I and FACSAria II, are over 15 and 13 years old, respectively. BD no longer supports
service contracts for the FACSAria I, and as a consequence, the instrument has been rendered mostly
inoperative. While the FACSAria II is still somewhat operational, its age and configuration (4 laser, 13 color, 4-
way sorting) are insufficient to meet current research needs. In addition, the FACSAria II is not housed within a
biosafety cabinet, which limits its use for sorting certain biohazardous samples, including some human clinical
samples. With these shortcomings recognized by senior MCC leadership, a comprehensive plan to revitalize the
FCSR was developed. Towards that end, they have appointed Dr. Signer as the new co-Director of the FCSR in
charge of new instrumentation. Funds are requested to acquire the BD FACSymphony S6 high parameter cell
sorter, a bench-top high speed cell sorter equipped with five lasers (355, 405, 488, 561, and 637 nm) capable of
analyzing up to 23 different colors plus forward and side scatter. The FACSymphony will be contained within a
Baker Class II Type A2 biosafety cabinet to meet safety and regulatory requirements for sorting clinical samples.
This instrument represents a crucial early step in advancing the MCC senior leaders’ vision to modernize the
MCC FCSR. The BD FACSymphony S6 cell sorter when combined with the expertise, leadership, and training
plans of Dr. Signer and staff will ensure that researchers at UCSD and within the surrounding scientific
community once again have access 24 hours a day, 7 days a week, 365 days a year to the cell sorting technology
they need to carry out high-impact cancer research. Without this instrument, the FCSR will continue to have
severely limited instrumentation, and MCC faculty research will be impaired. Acquisition of the BD
FACSymphony S6 cell sorter will enable the FCSR to continue its central mission to provide state-of-the-art
instrumentation, expert support, education, and training for MCC investigators and the La Jolla biomedical
research community in a highly effective, reliable and cost-efficient manner.
项目总结/文摘
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Robert A.J. Signer其他文献
3055 – ENHANCING TRANSLATION FIDELITY EXTENDS HEMATOPOIETIC STEM CELL LONGEVITY
- DOI:
10.1016/j.exphem.2024.104377 - 发表时间:
2024-08-01 - 期刊:
- 影响因子:
- 作者:
Amanda (AJ) Daniels;Xuezhen Ge;Mary Jean Sunshine;Daniela Dreifke;Marilyn Leonard;Yasar Kasu;Eric Bennett;Robert A.J. Signer - 通讯作者:
Robert A.J. Signer
Robert A.J. Signer的其他文献
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{{ truncateString('Robert A.J. Signer', 18)}}的其他基金
Ex vivo hematopoietic stem cell growth mediated by the heat shock response
热休克反应介导的离体造血干细胞生长
- 批准号:
10116376 - 财政年份:2020
- 资助金额:
$ 59.98万 - 项目类别:
Ex vivo hematopoietic stem cell growth mediated by the heat shock response
热休克反应介导的离体造血干细胞生长
- 批准号:
10544515 - 财政年份:2020
- 资助金额:
$ 59.98万 - 项目类别:
Ex vivo hematopoietic stem cell growth mediated by the heat shock response
热休克反应介导的离体造血干细胞生长
- 批准号:
10319623 - 财政年份:2020
- 资助金额:
$ 59.98万 - 项目类别:
Protein Homeostasis in Hematopoietic Stem Cells
造血干细胞中的蛋白质稳态
- 批准号:
10407580 - 财政年份:2018
- 资助金额:
$ 59.98万 - 项目类别:
Protein Homeostasis in Hematopoietic Stem Cells
造血干细胞中的蛋白质稳态
- 批准号:
10203945 - 财政年份:2018
- 资助金额:
$ 59.98万 - 项目类别:
Protein homeostasis in hematopoietic stem cells
造血干细胞中的蛋白质稳态
- 批准号:
10660341 - 财政年份:2018
- 资助金额:
$ 59.98万 - 项目类别:
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