Explore the words cloud of the NiSAN project. It provides you a very rough idea of what is the project "NiSAN" about.
The following table provides information about the project.
Coordinator |
BAR ILAN UNIVERSITY
Organization address contact info |
Coordinator Country | Israel [IL] |
Total cost | 149˙566 € |
EC max contribution | 149˙566 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2017-PoC |
Funding Scheme | ERC-POC |
Starting year | 2017 |
Duration (year-month-day) | from 2017-11-01 to 2019-04-30 |
Take a look of project's partnership.
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1 | BAR ILAN UNIVERSITY | IL (RAMAT GAN) | coordinator | 149˙566.00 |
To understand how the brain works, tools need to be developed to allow the investigation of interactions between individual neurons. Towards this goal, We developed voltage sensing nanoparticles (vsNPs) in the shape of nanorods (vsNRs) that self-insert into the cell membrane and could optically record, non-invasively, action potentials (APs) at the single-particle and nanoscale level, at multiple sites, in a large field-of-view. The proposed nanosensors have unique advantages not offered by other methods: much larger voltage sensitivity, high brightness, and hence single-particle voltage sensitivity, large spectral shift , fast temporal response, minimal photobleaching, large two-photon excitation cross sections, excellent performance in the NIR, and compatibility with lifetime imaging. In this PoC proposal we seek to convert the NVS program from mainly “R” in R&D effort into “D” effort which will allow for IP protection, commercialization, dissemination, and therefore the ‘democratization’ of the technology to the large community of neuroscientists. In order to convert our achievement to commercially viable reagents business for the neuroscience community via the PoC program, we will (i) identify leading applications in neuroscience and brain research, (ii) improve current technology to meet the applications demands by fine tuning the control over size and shape of the particle and testing various types of coating, testing insertion into different lipid compositions in bilayers and cells, and by testing non-specific internalization, (iii) improve the stability and performance reproducibility of the sensors, (iv) develop methods for upscaling the synthesis of these NPs, (v) and formulate GLP protocols required for commercialization.
Upon achievement of these goals, we will obtain a versatile, stable, multipurpose, novel tool to be implemented in neuroscience.
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The information about "NISAN" are provided by the European Opendata Portal: CORDIS opendata.