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Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse

Intrinsic optical signal imaging (ISI) is a hemodynamic response-based technique to map the functional architecture of the cortex. ISI is often used as an auxiliary method to localize cortical areas for targeted electrophysiology, pharmacology, or imaging experiments. Here, we provide a protocol for...

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Autores principales: Augustinaite, Sigita, Kuhn, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413905/
https://www.ncbi.nlm.nih.gov/pubmed/34505087
http://dx.doi.org/10.1016/j.xpro.2021.100779
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author Augustinaite, Sigita
Kuhn, Bernd
author_facet Augustinaite, Sigita
Kuhn, Bernd
author_sort Augustinaite, Sigita
collection PubMed
description Intrinsic optical signal imaging (ISI) is a hemodynamic response-based technique to map the functional architecture of the cortex. ISI is often used as an auxiliary method to localize cortical areas for targeted electrophysiology, pharmacology, or imaging experiments. Here, we provide a protocol for ISI through a cranial window with an access port to identify the area of the primary visual cortex (V1) in a head-fixed mouse, followed by targeted viral vector injection, which enables subsequent two-photon imaging of V1 layer 6 corticothalamic neurons. For complete details on the use and execution of this protocol, please refer to our paper Augustinaite and Kuhn (2020b).
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spelling pubmed-84139052021-09-08 Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse Augustinaite, Sigita Kuhn, Bernd STAR Protoc Protocol Intrinsic optical signal imaging (ISI) is a hemodynamic response-based technique to map the functional architecture of the cortex. ISI is often used as an auxiliary method to localize cortical areas for targeted electrophysiology, pharmacology, or imaging experiments. Here, we provide a protocol for ISI through a cranial window with an access port to identify the area of the primary visual cortex (V1) in a head-fixed mouse, followed by targeted viral vector injection, which enables subsequent two-photon imaging of V1 layer 6 corticothalamic neurons. For complete details on the use and execution of this protocol, please refer to our paper Augustinaite and Kuhn (2020b). Elsevier 2021-08-31 /pmc/articles/PMC8413905/ /pubmed/34505087 http://dx.doi.org/10.1016/j.xpro.2021.100779 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Augustinaite, Sigita
Kuhn, Bernd
Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title_full Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title_fullStr Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title_full_unstemmed Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title_short Intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
title_sort intrinsic optical signal imaging and targeted injections through a chronic cranial window of a head-fixed mouse
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413905/
https://www.ncbi.nlm.nih.gov/pubmed/34505087
http://dx.doi.org/10.1016/j.xpro.2021.100779
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