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MAGNEURON project deliverables

The page lists 19 deliverables related to the research project "MAGNEURON".

 List of Deliverables

MAGNEURON: list of downloadable deliverables.
title and desprition type last update

Consolidated Data Management Plan

Updated Data Management Plan will be consolidated at the end of the project.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Open Research Data Pilot 2020-04-16

Identification and assessment of neuronal differentiation and axonal outgrowth

Cells will be identified using immunocytochemistry with the following specific antibodies: to assess neuronal differentiation - beta-III-tubulin, Map2ab; and midbrain dopaminergic neurons – tyrosine hydroxylase, vesicular monoamine transporter (VMAT), dopamine transporter, Aromatic L-amino acid decarboxylase (AADC), and Nurr1. Axonal outgrowth will be measured and quantified from digital images of beta-III-tubulin labeled cells.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Dissemination Strategy report 2

This document will report on the dissemination and communication activities carried out in the period from M13 to M30 by the MAGNEURON consortium, with regard to the described communication activities in DoA.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Systematic analysis of the cell differentiation response to signalling perturbations

In vitro tests to define the differentiation responses of dopamine neurons in culture and in 3D systems including brain slices. Different regimes in 2D and 3D will be tested and optimized to promote neuronal regeneration.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Protocols for activation of neuronal differentiation through key receptor tags

Key receptors will be tested which can control neuronal cell differentiation e.g. TREK channels, Fz receptors. Magnetic particles will be coated with receptor tags and attached to receptors on the cell membrane. In response to oscillating fields, the cells will be induced to differentiate in vitro.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Final workshop

The final workshop will allow communicating the project results to a large scientific and industrial community.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Device for parallelized stimulation and high-throughput assay

We will develop a device for parallelized magnetic stimulation of multiple cells, based on microfabrication of micromagnets combined to micropatterning, enabling high-throughput assays. We will characterize the magnetic and optical performances of the devices.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Demonstrators, pilots, prototypes 2020-04-16

Final Dissemination Strategy report

This document will report on the dissemination and communication activities carried out in the period from M31 to M48 by the MAGNEURON consortium, with regard to the described communication activities in DoA.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-16

Characterization of magnetic manipulation in cells

We will characterize the forces required to manipulate cells inside cells, the kinetics with which they can be displaced through the cells. These results will be analyzed as a function of the colloidal and biofunctional properties of the nanoparticles.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Recombinant ferritin-based MNPs

We will deliver a protocol describing (i) expression and purification of recombinant ferritin particles, (ii) loading with magnetic iron oxide core and (iii) biochemical functionalization of magneto ferritin particles.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Intermediate workshop

The MAGNEURON consortium will organise an intermediate workshop during the project to communicate the intermediate results and generate synergies with the scientific community.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Dispersions of silica core shell MNPs

D2.2 is dedicated to the coating of maghemite nanoparticles synthesized in task 1 by a silica shell. If this synthesis pathway is well established for smaller particles, the protocol must be adapted to the big (12-14, up to 20 nm) ones that will be used in this project. Amines functional groups will be included on the surface of core-shell nanoparticles so as to be used by the other members of the consortium. Near infrared Fluorescent probes (Cyanine 5,5 for instance) will be included in the silica shell during synthesis for optical detection of nanoparticles in cells.
The quantities deliverables will be in the magnitude of 20-50 mL at 0.1 M of iron content. Sample should be available in the first 6-8 months after the beginning of the project.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Activation of intracellular membrane-anchored small G-proteins by cytosolic MNPs

MNPs functionalized with activated Ras/Rac (or their GEF activators) will be delivered into the cytoplasm of cells transfected with biosensors (Raichu-Ras, Raichu-Rac). Using the spaceMode approach, we will test for asymmetrical activation of downstream cytoskeletal targets using confocal fluorescence microscopy. Nonfunctionalized MNP will serve as negative control.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Dispersions of stabilized MNPs

This deliverable is synthesized big magnetic nanoparticles (from 12-14 and up to 20 nm in diameter) using an alternative Massart’s synthesis pathway. The necessary size sorting will be achieved in order to gain in monodispersity. For the full project, 200 mL at 1M of iron content is expected for each diameter selected. This will need several synthesis batches, as long as size sorting decreases strongly the quantity of expected nanoparticles.
Concomitantly, different coatings will be applied to these nanoparticles. Citrate ligands, as well as poly(sodium acrylate) (PAA) and poly(sodium acrylate-co-sodium maleate) (PAAMA) polyelectrolytes will be used to stabilize these nanoparticles in biocompatible solvents. These coated nanoparticles will be used in task 2.2 and 2.3.
Sample should be available in the first 4 months after the beginning of the project.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Dissemination Strategy report 1

This document will report on the dissemination and communication activities carried out in the period from M1 to M12 by the MAGNEURON consortium, with regard to the described communication activities in DoA.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

Data Management Plan

Data Management Plan will be written on the base of the EC tool. All the non-sensitivity data will be stored in an open repository.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

MAGNEURON website

The MAGNEURON web site will provide public information about the project, its objectives, the partners, the advancements, and the organised workshop and provide an entry contact point with any industry or organism interested in the project results.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Websites, patent fillings, videos etc. 2020-04-07

Dissemination Strategy plan

This document will report on the dissemination and communication strategies implemented by the MAGNEURON consortium, with regard to the described communication activities in DoA. A consistent graphical chart will be proposed for communication and dissemination supports. It shall be consistent with the IPR strategy plan.

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07

MAGNEURON brochure

The MAGNEURON brochure will be a dissemination way with public information on the project activities, objectives and progress that will be distributed whenever possible. Quantity of printed brochures will be defined by the Dissemination Plan. The logo, the design and the graphical chart will be consistent with the Website and other communication supports (internal and external).

Programme: H2020-EU.1.2.1. - Topic(s): FETOPEN-RIA-2014-2015

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Documents, reports 2020-04-07