Flow Cytometry and Cell Sorting Core (Core 3)

流式细胞术和细胞分选核心(核心 3)

基本信息

项目摘要

Abstract Inflammation is a complex biological process that involves many changes in the cell composition of circulating immune cells as well as tissues and organs. Identifying these changes in cell number and ratios, the status of various states of cell differentiation and apoptosis, and the expression patterns of cytokines and the signaling molecules that regulate the downstream pathways is essential in studying the process of inflammation. Many of these changes can be closely monitored by flow cytometry and sorting, and various other techniques based on micro-fluidic biotechnology such as multiplex ELISA assays for proteins and real time PCR for RNA. Many of these assays require expensive equipment and technical expertise that is not affordable by junior investigators such as the Target Faculty in this COBRE proposal on Dietary Supplements and Inflammation. In addition, setting operating parameters correctly and data interpretation when using these techniques is often difficult and requires experienced operators dedicated to the technology. The Flow Cytometry and Cell Sorting Core, which will be housed in the established Instrumentation Research Facility (IRF) at the University of South Carolina School of Medicine, will provide all of the technology and expertise required to complete these types of experiments proposed by the Target Investigators on this COBRE proposal. This core will be supervised by the current Director of the Flow Cytometry lab. There will be two faculty members who are affiliated with the IRF available for assistance with experimental design, operation of equipment, and training on micro-fluidics instrumentation. In addition to individual interactions, didactic courses, seminars and workshops are often sponsored through the IRF. These will be made available to members of the Target Investigator laboratories.
摘要 炎症是一个复杂的生物过程,涉及循环免疫细胞以及组织和器官的细胞组成的许多变化。确定这些细胞数量和比例的变化,细胞分化和凋亡的各种状态,以及调节下游通路的细胞因子和信号分子的表达模式,对于研究炎症过程至关重要。这些变化中的许多可以通过流式细胞术和分选以及基于微流控生物技术的各种其他技术来密切监测,例如蛋白质的多重ELISA法和RNA的实时PCR分析。其中许多分析需要昂贵的设备和技术专业知识,这是初级研究人员(如科布雷关于膳食补充剂和炎症的科布雷提案中的塔吉特学院)负担不起的。此外,在使用这些技术时,正确设置操作参数和数据解释通常是困难的,需要有经验的操作员专门从事该技术。流式细胞术和细胞分选核心将设在南卡罗来纳大学医学院现有的仪器研究设施(IRF)中,它将提供完成目标研究人员就Cobre提案提出的这些类型实验所需的所有技术和专业知识。这一核心将由现任流式细胞仪实验室主任监督。将有两名隶属于IRF的教职员工,他们可以在实验设计、设备操作和微流体仪器培训方面提供帮助。除了个人互动,授课课程、研讨会和讲习班通常是通过国际扶轮基金会赞助的。这些资料将提供给目标调查员实验室的成员。

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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Udai P. Singh其他文献

The effects of heme modification on reactivity, ligand binding properties and iron-coordination structures of cytochrome P450nor.
血红素修饰对细胞色素 P450nor 反应性、配体结合特性和铁配位结构的影响。
  • DOI:
  • 发表时间:
    1998
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Udai P. Singh;Eiji Obayashi;Satoshi Takahashi;Tetsutaro Iizuka;Hirofumi Shoun;Y. Shiro
  • 通讯作者:
    Y. Shiro
Modulation of occludin, NF-κB, p-STAT3, and Th17 response by DJ-X-025 decreases inflammation and ameliorates experimental colitis
DJ - X - 025对闭合蛋白、核因子-κB、磷酸化信号转导及转录激活因子3和辅助性T细胞17反应的调节可减轻炎症并改善实验性结肠炎
  • DOI:
    10.1016/j.biopha.2025.117939
  • 发表时间:
    2025-04-01
  • 期刊:
  • 影响因子:
    7.500
  • 作者:
    Mousumi Mandal;Md Abdullah Al Mamun;Ahmed Rakib;Santosh Kumar;Frank Park;Dong-Jin Hwang;Wei Li;Duane D. Miller;Udai P. Singh
  • 通讯作者:
    Udai P. Singh
Preparation, X-ray crystallography and thermal decomposition of transition metal perchlorate complexes with perchlorate and 2,2′-bipyridyl ligands
  • DOI:
    10.1016/j.ica.2009.06.003
  • 发表时间:
    2009-08-15
  • 期刊:
  • 影响因子:
  • 作者:
    Gurdip Singh;Inder Pal Singh Kapoor;Dinesh Kumar;Udai P. Singh;Nidhi Goel
  • 通讯作者:
    Nidhi Goel
Interconversion of host–guest components in supramolecular assemblies of polycarboxylic acids and reduced Schiff bases
  • DOI:
    10.1007/s11224-015-0699-0
  • 发表时间:
    2015-12-07
  • 期刊:
  • 影响因子:
    2.200
  • 作者:
    Udai P. Singh;Kapil Tomar;Sujata Kashyap
  • 通讯作者:
    Sujata Kashyap
Device Performance Enhancement Using CTSe/CTSSe Bilayer Structure: A Numerical Analysis
使用 CTSe/CTSSe 双层结构增强器件性能:数值分析

Udai P. Singh的其他文献

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{{ truncateString('Udai P. Singh', 18)}}的其他基金

Adipose T cell microRNAs (miRs) regulate macrophage function during obesity
脂肪 T 细胞 microRNA (miR) 在肥胖期间调节巨噬细胞功能
  • 批准号:
    10221966
  • 财政年份:
    2020
  • 资助金额:
    $ 13.7万
  • 项目类别:
Adipose T cell microRNAs (miRs) regulate macrophage function during obesity
脂肪 T 细胞 microRNA (miR) 在肥胖期间调节巨噬细胞功能
  • 批准号:
    10335275
  • 财政年份:
    2020
  • 资助金额:
    $ 13.7万
  • 项目类别:
Adipose T cell microRNAs (miRs) regulate macrophage function during obesity
脂肪 T 细胞 microRNA (miR) 在肥胖期间调节巨噬细胞功能
  • 批准号:
    10240751
  • 财政年份:
    2020
  • 资助金额:
    $ 13.7万
  • 项目类别:
Immune Mechanism Underlying CXCR3 and its Ligand Mediated Interstitial Cystitis
CXCR3及其配体介导间质性膀胱炎的免疫机制
  • 批准号:
    8537713
  • 财政年份:
    2012
  • 资助金额:
    $ 13.7万
  • 项目类别:
Flow Cytometry and Cell Sorting Core (Core 3)
流式细胞术和细胞分选核心(核心 3)
  • 批准号:
    8531304
  • 财政年份:
  • 资助金额:
    $ 13.7万
  • 项目类别:
Flow Cytometry and Cell Sorting Core (Core 3)
流式细胞术和细胞分选核心(核心 3)
  • 批准号:
    9091637
  • 财政年份:
  • 资助金额:
    $ 13.7万
  • 项目类别:
Flow Cytometry and Cell Sorting Core (Core 3)
流式细胞术和细胞分选核心(核心 3)
  • 批准号:
    8460792
  • 财政年份:
  • 资助金额:
    $ 13.7万
  • 项目类别:
Flow Cytometry and Cell Sorting Core (Core 3)
流式细胞术和细胞分选核心(核心 3)
  • 批准号:
    8853883
  • 财政年份:
  • 资助金额:
    $ 13.7万
  • 项目类别:

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