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Article: Quantitative analysis of phosphoinositide 3-kinase (PI3K) signaling using live-cell total internal reflection fluorescence (TIRF) microscopy

TitleQuantitative analysis of phosphoinositide 3-kinase (PI3K) signaling using live-cell total internal reflection fluorescence (TIRF) microscopy
Authors
KeywordsCell biophysics
Cell migration
Image analysis
Image processing
Signal transduction
Issue Date2013
Citation
Current Protocols in Cell Biology, 2013, suppl. 61, p. 14.14.1-14.14.24 How to Cite?
AbstractThis unit focuses on the use of total internal reflection fluorescence (TIRF) microscopy and image analysis methods to study the dynamics of signal transduction mediated by class I phosphoinositide 3-kinases (PI3Ks) in mammalian cells. The first four protocols cover live-cell imaging experiments, image acquisition parameters, and basic image processing and segmentation. These methods are generally applicable to livecell TIRF experiments. The remaining protocols outline more advanced image analysis methods, which were developed in our laboratory for the purpose of characterizing the spatiotemporal dynamics of PI3K signaling. These methods may be extended to analyze other cellular processes monitored using fluorescent biosensors. © 2013 by John Wiley & Sons, Inc.
Persistent Identifierhttp://hdl.handle.net/10722/311385
ISSN
2023 SCImago Journal Rankings: 1.872

 

DC FieldValueLanguage
dc.contributor.authorJohnson, Heath E.-
dc.contributor.authorHaugh, Jason M.-
dc.date.accessioned2022-03-22T11:53:48Z-
dc.date.available2022-03-22T11:53:48Z-
dc.date.issued2013-
dc.identifier.citationCurrent Protocols in Cell Biology, 2013, suppl. 61, p. 14.14.1-14.14.24-
dc.identifier.issn1934-2500-
dc.identifier.urihttp://hdl.handle.net/10722/311385-
dc.description.abstractThis unit focuses on the use of total internal reflection fluorescence (TIRF) microscopy and image analysis methods to study the dynamics of signal transduction mediated by class I phosphoinositide 3-kinases (PI3Ks) in mammalian cells. The first four protocols cover live-cell imaging experiments, image acquisition parameters, and basic image processing and segmentation. These methods are generally applicable to livecell TIRF experiments. The remaining protocols outline more advanced image analysis methods, which were developed in our laboratory for the purpose of characterizing the spatiotemporal dynamics of PI3K signaling. These methods may be extended to analyze other cellular processes monitored using fluorescent biosensors. © 2013 by John Wiley & Sons, Inc.-
dc.languageeng-
dc.relation.ispartofCurrent Protocols in Cell Biology-
dc.subjectCell biophysics-
dc.subjectCell migration-
dc.subjectImage analysis-
dc.subjectImage processing-
dc.subjectSignal transduction-
dc.titleQuantitative analysis of phosphoinositide 3-kinase (PI3K) signaling using live-cell total internal reflection fluorescence (TIRF) microscopy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/0471143030.cb1414s61-
dc.identifier.pmid24510804-
dc.identifier.scopuseid_2-s2.0-84896330579-
dc.identifier.issuesuppl. 61-
dc.identifier.spage14.14.1-
dc.identifier.epage14.14.24-
dc.identifier.eissn1934-2616-

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