PROTEOMICS OF CHERNO

"The quantitative proteomics analysis of developing embryo, endosperm and seed coat in control and Chernobyl-grown plants"

 Coordinatore INSTITUTE OF PLANT GENETICS AND BIOTECHNOLOGY 

 Organization address city: NITRA
postcode: 95007

contact info
Titolo: Prof.
Nome: Anna
Cognome: Pret'ová
Email: send email
Telefono: -7336275
Fax: -7337118

 Nazionalità Coordinatore Slovakia [SK]
 Totale costo 100˙000 €
 EC contributo 100˙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-2007-4-3-IRG
 Funding Scheme MC-IRG
 Anno di inizio 2007
 Periodo (anno-mese-giorno) 2007-09-03   -   2011-09-02

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUTE OF PLANT GENETICS AND BIOTECHNOLOGY

 Organization address city: NITRA
postcode: 95007

contact info
Titolo: Prof.
Nome: Anna
Cognome: Pret'ová
Email: send email
Telefono: -7336275
Fax: -7337118

SK (NITRA) coordinator 0.00

Mappa


 Word cloud

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reference    chernobyl    power    seed    ms    nuclear    maps    plant    protein   

 Obiettivo del progetto (Objective)

'With each passing year since Chernobyl accident, more questions arise about the potential for organisms adapt to radiation exposure. The explosion of one of the four reactors of Chernobyl nuclear power plant on 26 April 1986 caused worst environmental nuclear disaster in the history. It transported vast amounts of radioactive material into the atmosphere, much of which was subsequently deposited not only in the immediate vicinity of power plant in Ukraine, Belarus and Russia, but over the large parts of Europe. In this proposal, quantitative protein reference maps will be used to identify differentially expressed proteins in developing embryo, endosperm and seed coats of Chernobyl-grown plants compared to control. These reference maps will be generated during five stages of soybean and flax seed development using two-dimensional electrophoresis (2-DE) in combination with liquid chromatography connected with tandem mass spectrometry (LC-MS/MS) for protein identification.'

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