Protocol to image and analyze hippocampal network dynamics in non-anesthetized mouse pups
Résumé
Two-photon calcium imaging is a powerful technique that has revolutionized our understanding of how neural circuit dynamics supports different behaviors and cognitive processes. However, performing imaging during development remains challenging. Here, we provide a protocol to image CA1 neurons in mouse pups as well as a pipeline of analysis to analyze and share the data. We describe steps for intracerebroventricular injection, cranial window surgery, two-photon calcium imaging, and analysis of imaging data.
Domaines
NeurobiologieOrigine | Fichiers éditeurs autorisés sur une archive ouverte |
---|---|
Licence |