Amb motiu del tancament d'estiu, la validació de documents es reprendrà a partir del 28 d'agost de 2026. Disculpeu les molèsties.
Con motivo del cierre de verano, la validación de documentos se reanudará a partir del 28 de agosto de 2026. Disculpad las molestias
Due to the summer closure, document validation will resume starting August 28, 2026. We apologize for any inconvenience.

Files

Bouchier-HayesL.pdf (168.16 KB)

Document type

Article

Version

Accepted version

Publication date

2008-03

All rights reserved

Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/126415

Measuring apoptosis at the single cell level

Journal Title

Authors

Director/Tutor

Journal ISSN

Volume Title

Related resource

https://doi.org/10.1016/j.ymeth.2007.11.007

Abstract

The use of live cell microscopy has made a number of contributions to the study of apoptosis. Many of the tools and techniques are available that allow us to image the key events that occur during cell death including mitochondrial outer membrane permeabilization, mitochondrial transmembrane potential changes, translocation of Bcl-2 family members, caspase activation, phosphatidylserine flip and plasma membrane rupture. We discuss these techniques here and highlight the advantages and drawbacks of using such approaches to study apoptosis. (C) 2007 Elsevier Inc. All rights reserved.

Subject

Apoptosi, Microscòpia confocal

Subject (English)

Apoptosis, Confocal microscopy

Citation

Collections

Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

Citation

BOUCHIER-HAYES, Lisa, et al. Measuring apoptosis at the single cell level. Methods. 2008. Vol. 44, num. 3, pags. 222-228. [consulted: 14 of August of 2026]. Available at: https://hdl.handle.net/2445/126415

Export metadata

JSON - METS

Share record