HICONTCELLSCREEN

Development of systems for high content screening of live cells

 Coordinatore TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY 

 Organization address address: TECHNION CITY - SENATE BUILDING
city: HAIFA
postcode: 32000

contact info
Titolo: Mr.
Nome: Mark
Cognome: Davison
Email: send email
Telefono: -8293886
Fax: -8231990

 Nazionalità Coordinatore Israel [IL]
 Totale costo 50˙000 €
 EC contributo 50˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2009-RG
 Funding Scheme MC-IRG
 Anno di inizio 0
 Periodo (anno-mese-giorno) 0000-00-00   -   0000-00-00

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY

 Organization address address: TECHNION CITY - SENATE BUILDING
city: HAIFA
postcode: 32000

contact info
Titolo: Mr.
Nome: Mark
Cognome: Davison
Email: send email
Telefono: -8293886
Fax: -8231990

IL (HAIFA) coordinator 50˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

hcs    culture    involves    primary    network    biology    screening    cells    cell   

 Obiettivo del progetto (Objective)

'Light microscopy has many applications in the life and health sciences. These applications include drug screening, in vitro fertilization, medical diagnostics and basic research in cell and systems biology [ref]. Many of these applications require the imaging of multiple samples over extended periods of times using a methodology that is often referred to as High Content Screening (HCS). Systems for performing HCS do exist, however thes systems generally provide a solution for a limited range of problems. Consequently there are many systems for which no suitable HCS technology is available. The first system involves a culture of primary naïve T-cells in conjunction with antigen presenting dendritic cells (APCs), which is used for studying the biology of T-cell activation. The second system involves nvolves the culture of primary rat neurons transfected to express fluorescently labelled synapse markers on Multi-Electrode Arrays (MEAs) dishes. This system is being used to study the connection between neural network structure and the electric activity of the network. We propose to develop novel software and hardware technology that will enable efficient research using these systems.'

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