BIOASSAYDEVICE

A device for biological high-throughput assays based on in vitro compartmentalisation

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE 

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Wendy
Cognome: Holman
Email: send email
Telefono: 441223000000
Fax: 441224000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 178˙874 €
 EC contributo 178˙874 €
 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-2007-4-2-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-03-01   -   2010-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF CAMBRIDGE

 Organization address address: The Old Schools, Trinity Lane
city: CAMBRIDGE
postcode: CB2 1TN

contact info
Titolo: Ms.
Nome: Wendy
Cognome: Holman
Email: send email
Telefono: 441223000000
Fax: 441224000000

UK (CAMBRIDGE) coordinator 0.00

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 Word cloud

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

proteins    assays    protein    functional    biological    microfluidic    chip   

 Obiettivo del progetto (Objective)

'The vision of putting a lab on a chip has far reaching implications for biological research. Microfluidic systems can now be built that - for example in past research by the applicant - can be used for protein crystallisation with only minute amount of precious proteins. A second challenge is to carry out functional biological assays on a chip. Such assays are used in high-throughput screening, e.g. for novel drug molecule or protein mutants with improved properties for directed evolution of functional proteins. In each case the economy of the assay system (total numbers screened, speed, reliability, quality of the kinetic readout) will crucially determine the success of this combinatorial approach. Water-in-oil droplets within microfluidic channels have the potential to serve as isolated reaction compartments, just like natural cells. Their femtolitre volumes minimise sample consumption and eliminate dispersion of substrates or products. To this end the candidate will build novel microfluidic devices that incoproprate the principle of in vitro compartementalisation. The fabrication of this device, and especially the integration of the various components is a significant challenge.'

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