Upgrading the CVID Biosensor Core Facility with a Biacore 8K instrument
Upgrading the CVID Biosensor Core Facility with a Biacore 8K instrument
批准号:
10176937
负责人:
Dudley K. Strickland
金额:
$43.89万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-07-01 至 2022-06-30
关键词:
AttentionBiologyBiosensorBlood VesselsCommunitiesCore FacilityDiseaseExperimental DesignsFundingGenesGenomicsHomeInflammatoryLabelMarylandMeasuresMinorMolecular WeightPeer ReviewPhysiologicalProteomicsPublicationsReproducibilityResearchResourcesSurface Plasmon ResonanceSystemTechnologyUniversitiesbiomedical resourcegene productinnovationinstrumentmedical schools
中文摘要
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英文摘要
Project Summary/Abstract
As tremendous advances have occurred in genomic biology, gene sequencing technologies, and
proteomic technologies, attention is increasingly focusing on gene products, most of which
function by interacting with other gene products. A comprehensive understanding of physiological
systems requires an in-depth definition of quantitative interactions between molecules. Biosensor
technologies provides a powerful approach to define these interactions in label-free systems.
Here we seek funds to upgrade the Biosensor Core facility in the Center of Vascular and
Inflammatory Diseases (CVID) at the University of Maryland School of Medicine by the purchase
of a Biacore 8K instrument. The major users of this Core have extensive expertise employing
surface plasmon resonance technology with over 45 peer-reviewed publications employing the
technology. The new instrument (Biacore 8K) will be integrated into the CVID Biosensor Core
Facility and with the Center for Innovative Biomedical Resources (CIBR), the Administrative home
for the University of Maryland School of Medicine Core facilities, thus providing the resource for
our growing research community. The Biacore 8K will enhance the research of the Major users
and Minor users by increasing the throughput capacity, by enhancing a more reproducible and
optimized experimental design, and by increasing the sensitivity for measuring the interaction of
low molecular weight molecules.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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财政年份:2017
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依托单位:
Role of LDL receptor family members in protecting the vasculature
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批准号:10078621
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资助金额:$77.25万
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财政年份:2017
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Role of LDL receptor family members in protecting the vasculature
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批准号:10532199
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资助金额:$77.25万
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依托单位:
Mechanisms by which LRP1 Protects the Vasculature
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批准号:8722143
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资助金额:$38.38万
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财政年份:2014
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Role of Lipoprotein Receptors in Venous Thrombosis
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批准号:8435382
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资助金额:$36.53万
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财政年份:2012
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负责人:Dudley K. Strickland
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依托单位:
Role of Lipoprotein Receptors in Venous Thrombosis
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批准号:8320618
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资助金额:$38.38万
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财政年份:2012
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依托单位:
Role of Lipoprotein Receptors in Venous Thrombosis
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批准号:8814273
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资助金额:$37.8万
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财政年份:2012
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负责人:Dudley K. Strickland
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依托单位:
Role of Lipoprotein Receptors in Venous Thrombosis
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批准号:8623147
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项目类别:
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资助金额:$37.61万
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财政年份:2012
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负责人:Dudley K. Strickland
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依托单位:
Administrative Core
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批准号:7264692
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资助金额:$8.32万
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财政年份:2007
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负责人:Dudley K. Strickland
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依托单位:
Lipoprotein Receptors and Inflammation in the Vessel Wall
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批准号:7264687
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项目类别:
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资助金额:$42.94万
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负责人:Dudley K. Strickland
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依托单位:
Xth International Workshop on Plasminogen Activation
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依托单位:
Prolongation of Factor VIII Lifetime in Circulation
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批准号:7035373
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项目类别:
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资助金额:$36.25万
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财政年份:2003
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负责人:Dudley K. Strickland
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依托单位:
LRP mediated cellular signaling events
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批准号:6644329
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项目类别:
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财政年份:2002
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负责人:Dudley K. Strickland
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依托单位:
BIACORE 3000 SURFACE PLASMON RESONANCE INSTRUMENT
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批准号:6292013
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项目类别:
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资助金额:$26.0万
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财政年份:2001
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负责人:Dudley K. Strickland
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依托单位:
FUNCTIONAL STUDIES ON THE VERY LOW DENSITY LIPOPROTEIN RECEPTOR
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资助金额:$18.72万
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财政年份:2000
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HIV PROTEASE INHIBITOR & LIPOPROTEIN RECEPTOR IMPAIRMENT
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资助金额:$26.99万
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财政年份:2000
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依托单位:
HIV PROTEASE INHIBITOR & LIPOPROTEIN RECEPTOR IMPAIRMENT
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批准号:6612671
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资助金额:$26.99万
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财政年份:2000
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负责人:Dudley K. Strickland
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依托单位:
HIV PROTEASE INHIBITOR & LIPOPROTEIN RECEPTOR IMPAIRMENT
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批准号:6537903
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资助金额:$26.99万
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财政年份:2000
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负责人:Dudley K. Strickland
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依托单位:
6TH RESEARCH CONFERENCE ON THROMBOLYSIS
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批准号:6089058
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项目类别:
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资助金额:$1.0万
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财政年份:2000
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负责人:Dudley K. Strickland
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依托单位:
国内基金
海外基金
Journal of Integrative Plant Biology
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批准号:31024801
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批准年份:2010
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依托单位: