JoVE Encyclopedia of Experiments
Neuroscience
0 views • 3:30 min • July 8th, 2025
This article presents a detailed protocol for the prolonged incubation of acute neuronal tissue from the mouse retina, enabling subsequent electrophysiological and calcium imaging studies. The method involves enzymatic removal of the inner limiting membrane (ILM), careful tissue handling, and incubation in a specialized system designed to preserve tissue viability and prevent microbial contamination.
Prolonged incubation of retinal neuronal tissue enables extended viability for ex vivo functional studies, directly supporting early discovery and mechanistic de-risking in neuropharma pipelines. This capability enhances predictive confidence in electrophysiological and imaging assays, facilitating robust target validation and reducing biological ambiguity at critical decision points. Reliable preservation of tissue integrity underpins translational continuity and portfolio prioritization for CNS and retinal drug discovery programs.
This incubation technique fits at the interface of early discovery and lead identification, enabling reliable functional assays and supporting preclinical model development for CNS and retinal programs.
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Last updated: 1 August 2026