Imaging amyloid precursor protein in vivo: An axonal transport assay
- Autores
- Falzone, Tomas Luis; Stokin, Gorazd B.
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Fusion of fluorescent probes to axonally transported proteins represents an established approach that enables live imaging of axonal transport. In this approach, in vivo examination of fluorescent particle dynamics provides information about the length, directionality, and the velocity by which axonally transported proteins travel along axons. Analysis of these parameters provides information about the distribution of axonal proteins and their dynamics in and between different subcellular compartments. Establishing the movement behavior of amyloid precursor protein within axons indicated that live imaging approaches offer the opportunity to significantly enhance our understanding of the biology as well as pathology of axonal transport. This chapter provides a fluorescence-based procedure for measuring axonal transport of APP in cultured newborn mouse hippocampal neurons. © 2012 Springer Science+Business Media, LLC.
Fil: Falzone, Tomas Luis. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencias; Argentina
Fil: Stokin, Gorazd B.. University Medical Center; Eslovenia - Materia
-
Amyloid Precursor Protein
Axonal Transport
Fluorescent Probes
In Vivo Fluorescent Imaging
Primary Hippocampal Cell Culture - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/67300
Ver los metadatos del registro completo
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Imaging amyloid precursor protein in vivo: An axonal transport assayFalzone, Tomas LuisStokin, Gorazd B.Amyloid Precursor ProteinAxonal TransportFluorescent ProbesIn Vivo Fluorescent ImagingPrimary Hippocampal Cell Culturehttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Fusion of fluorescent probes to axonally transported proteins represents an established approach that enables live imaging of axonal transport. In this approach, in vivo examination of fluorescent particle dynamics provides information about the length, directionality, and the velocity by which axonally transported proteins travel along axons. Analysis of these parameters provides information about the distribution of axonal proteins and their dynamics in and between different subcellular compartments. Establishing the movement behavior of amyloid precursor protein within axons indicated that live imaging approaches offer the opportunity to significantly enhance our understanding of the biology as well as pathology of axonal transport. This chapter provides a fluorescence-based procedure for measuring axonal transport of APP in cultured newborn mouse hippocampal neurons. © 2012 Springer Science+Business Media, LLC.Fil: Falzone, Tomas Luis. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencias; ArgentinaFil: Stokin, Gorazd B.. University Medical Center; EsloveniaHumana Press2012-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/67300Falzone, Tomas Luis; Stokin, Gorazd B.; Imaging amyloid precursor protein in vivo: An axonal transport assay; Humana Press; Methods in Molecular Biology; 846; 8-2012; 295-3031064-3745CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1007/978-1-61779-536-7_25info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/protocol/10.1007%2F978-1-61779-536-7_25info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:51:59Zoai:ri.conicet.gov.ar:11336/67300instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:51:59.599CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
title |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
spellingShingle |
Imaging amyloid precursor protein in vivo: An axonal transport assay Falzone, Tomas Luis Amyloid Precursor Protein Axonal Transport Fluorescent Probes In Vivo Fluorescent Imaging Primary Hippocampal Cell Culture |
title_short |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
title_full |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
title_fullStr |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
title_full_unstemmed |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
title_sort |
Imaging amyloid precursor protein in vivo: An axonal transport assay |
dc.creator.none.fl_str_mv |
Falzone, Tomas Luis Stokin, Gorazd B. |
author |
Falzone, Tomas Luis |
author_facet |
Falzone, Tomas Luis Stokin, Gorazd B. |
author_role |
author |
author2 |
Stokin, Gorazd B. |
author2_role |
author |
dc.subject.none.fl_str_mv |
Amyloid Precursor Protein Axonal Transport Fluorescent Probes In Vivo Fluorescent Imaging Primary Hippocampal Cell Culture |
topic |
Amyloid Precursor Protein Axonal Transport Fluorescent Probes In Vivo Fluorescent Imaging Primary Hippocampal Cell Culture |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Fusion of fluorescent probes to axonally transported proteins represents an established approach that enables live imaging of axonal transport. In this approach, in vivo examination of fluorescent particle dynamics provides information about the length, directionality, and the velocity by which axonally transported proteins travel along axons. Analysis of these parameters provides information about the distribution of axonal proteins and their dynamics in and between different subcellular compartments. Establishing the movement behavior of amyloid precursor protein within axons indicated that live imaging approaches offer the opportunity to significantly enhance our understanding of the biology as well as pathology of axonal transport. This chapter provides a fluorescence-based procedure for measuring axonal transport of APP in cultured newborn mouse hippocampal neurons. © 2012 Springer Science+Business Media, LLC. Fil: Falzone, Tomas Luis. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencias; Argentina Fil: Stokin, Gorazd B.. University Medical Center; Eslovenia |
description |
Fusion of fluorescent probes to axonally transported proteins represents an established approach that enables live imaging of axonal transport. In this approach, in vivo examination of fluorescent particle dynamics provides information about the length, directionality, and the velocity by which axonally transported proteins travel along axons. Analysis of these parameters provides information about the distribution of axonal proteins and their dynamics in and between different subcellular compartments. Establishing the movement behavior of amyloid precursor protein within axons indicated that live imaging approaches offer the opportunity to significantly enhance our understanding of the biology as well as pathology of axonal transport. This chapter provides a fluorescence-based procedure for measuring axonal transport of APP in cultured newborn mouse hippocampal neurons. © 2012 Springer Science+Business Media, LLC. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-08 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/67300 Falzone, Tomas Luis; Stokin, Gorazd B.; Imaging amyloid precursor protein in vivo: An axonal transport assay; Humana Press; Methods in Molecular Biology; 846; 8-2012; 295-303 1064-3745 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/67300 |
identifier_str_mv |
Falzone, Tomas Luis; Stokin, Gorazd B.; Imaging amyloid precursor protein in vivo: An axonal transport assay; Humana Press; Methods in Molecular Biology; 846; 8-2012; 295-303 1064-3745 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1007/978-1-61779-536-7_25 info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/protocol/10.1007%2F978-1-61779-536-7_25 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Humana Press |
publisher.none.fl_str_mv |
Humana Press |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842269128683945984 |
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13.13397 |