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dc.contributor.authorKong, B.-
dc.contributor.authorYang, Y.-
dc.contributor.authorKweon, D.-H.-
dc.date.accessioned2024-02-21T05:03:15Z-
dc.date.available2024-02-21T05:03:15Z-
dc.date.issued2019-
dc.identifier.issn1064-3745-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/148754-
dc.description.abstractDynamic light scattering (DLS) spectroscopy provides rapid information on the size distribution of a large number of particles in a mixture. Vesicle sizes change during the merger of lipid bilayers, and DLS analysis can provide rapid, accurate, and non-perturbative quantification of the size distribution of proteoliposomes in SNARE-dependent membrane fusion. In this chapter, we describe the methodologies and reagents used for DLS spectroscopy in a biochemical and biophysical study of SNARE-mediated membrane fusion. ? Springer Science+Business Media, LLC, part of Springer Nature 2019.-
dc.language2-
dc.publisherHumana Press Inc.-
dc.titleDynamic light scattering analysis to dissect intermediates of SNARE-mediated membrane fusion-
dc.typeBook-
dc.identifier.doi10.1007/978-1-4939-8760-3_4-
dc.citation.startPage53-
dc.citation.endPage69-

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