RED-FPT

Red-Shifted Fluorescence Protein Tomography

 Coordinatore HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH 

 Organization address address: Ingolstaedter Landstrasse 1
city: MUENCHEN
postcode: 85764

contact info
Titolo: Mr.
Nome: Juergen
Cognome: Ertel
Email: send email
Telefono: +49 089 31873852
Fax: +490 89 31873017

 Nazionalità Coordinatore Germany [DE]
 Totale costo 162˙096 €
 EC contributo 162˙096 €
 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-2007-2-1-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-09-01   -   2010-10-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH

 Organization address address: Ingolstaedter Landstrasse 1
city: MUENCHEN
postcode: 85764

contact info
Titolo: Mr.
Nome: Juergen
Cognome: Ertel
Email: send email
Telefono: +49 089 31873852
Fax: +490 89 31873017

DE (MUENCHEN) coordinator 0.00

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imaging    proteins    animals    deep    optical    tomographic    cellular    fluorescent    tissue    small   

 Obiettivo del progetto (Objective)

'The introduction of transgenes that express fluorescent proteins (FPs) into cells has revolutionized the ability to visualize many cellular and sub-cellular processes that are otherwise invisible with traditional means of optical imaging. Fluorescent proteins have been widely used in microscopic imaging, however deep tissue imaging has not been possible, before the recent development of fluorescent proteins emitting beyond the 600 nm absorption threshold. In the present proposal the applicant will study and develop a novel optical tomographic method for preclinical research applications with the use of the recently evolved red-shifted fluorescent proteins. The development is going to be based on modifying the existing Fluorescence Molecular Tomography method both in its experimental and theoretical part as necessary. The result will be a tomographic method and system that will be used to reconstruct in 3D the location of the fluorescent proteins deep inside the tissue of small animals (mice) with submillimeter resolution. The proposed method/system will be tested against various of the parameters of its operation and will be used to demonstrate its use in in-vivo biomedical imaging applications. A method/system like the proposed has the potential to become a high capability non invasive monitoring and diagnostic tool in bio-medical research on small animals.'

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