Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/58774
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dc.contributor.authorKumar, S.-
dc.contributor.authorDorstyn, L.-
dc.date.issued2009-
dc.identifier.citationMethods in Molecular Biology, 2009, vol.559, pp.3-17-
dc.identifier.isbn9781603270168-
dc.identifier.urihttp://hdl.handle.net/2440/58774-
dc.description.abstractApoptotic cell death is characterised by various morphological and biochemical changes. Cysteine proteases of the caspase family play key roles in the execution of apoptosis and in the maturation of proinflammatory cytokines. During apoptosis signalling, caspase precursors undergo rapid proteolytic processing and activation. Activated caspases then function to cleave various vital cellular proteins, resulting in the death of the cell. Thus, the measurement of caspase activation and caspase activity provides a quick and convenient method to assess apoptosis. This chapter outlines various commonly used assays for measuring caspase activity and detecting active caspases in cultured cells or tissue extracts.-
dc.description.statementofresponsibilitySharad Kumar and Loretta Dorstyn-
dc.language.isoen-
dc.publisherHumana Press, Inc.-
dc.rights© Humana Press, a part of Springer Science + Business Media, LLC 2004, 2009-
dc.subjectApoptosis-
dc.subjectCaspase activation-
dc.subjectSynthetic peptides-
dc.subjectElectrophoresis-
dc.subjectImmunoblotting-
dc.titleAnalysing caspase activation and caspase activity in apoptotic cells-
dc.typeBook chapter-
dc.identifier.doi10.1007/978-1-60327-017-5_1-
pubs.publication-statusPublished-
dc.identifier.orcidKumar, S. [0000-0001-7126-9814]-
Appears in Collections:Aurora harvest 5
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