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| Funder | National Centre for the Replacement, Refinement and Reduction of Animals in Research |
|---|---|
| Recipient Organization | MRC London Institute of Medical Sciences |
| Country | United Kingdom |
| Start Date | Oct 01, 2024 |
| End Date | Mar 14, 2025 |
| Duration | 164 days |
| Number of Grantees | 1 |
| Roles | Award Holder |
| Data Source | Europe PMC |
| Grant ID | APP51121 |
The MRC LMS seeks £90,000 to evaluate non-animal derived products across several workflows throughout the institute.
The LMS, an internationally renowned research institute, is dedicated to cutting-edge research while reducing animal-intensive research for ethical and environmental reasons. Transitioning to non-animal derived products is the next logical step.
A significant barrier to adopting non-animal reagents is the resources and effort required for testing and optimization.
Therefore, we request funds to support the purchase and validation of non-animal derived products for four key projects within the LMS.
These projects will focus on our Flow Cytometry, Proteomics, and Microscopy facilities, as well as our central Tissue Culture protocols.
Specifically, we aim to validate non-animal derived antibodies for FACs, immunofluorescence imaging, and proteomics, and to assess their efficacy when combined with animal-free media used in generating samples for these assays.
This initiative will encompass a wide range of non-animal products for our most commonly used protocols and facilitate their adoption by other research groups.
Additionally, we plan to share our findings with other UK and international institutes to promote the global adoption of animal-free protocols.
Validating and testing are resource-intensive processes; therefore, we plan to combine these projects with internally funded graduate initiatives, providing bespoke product testing tailored to individual research needs over 6-12 months.
This approach ensures direct input from our research groups, fostering trust in the results and ensuring that successful products will be incorporated into central protocols.
By providing our researchers with the necessary time and resources to test these products, we will remove current barriers that hinder their use and establish significant changes to our most common workflows.
MRC London Institute of Medical Sciences
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