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dc.contributor.advisorCloninger, Mary
dc.contributor.authorGoodman, Candace
dc.date.accessioned2013-03-05T18:51:46Z
dc.date.available2013-03-05T18:51:46Z
dc.date.issued2013-03
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/480
dc.descriptionAbstract Onlyen_US
dc.description.abstractThe ability to characterize aggregation is significant in developing a mechanistic understanding of the process and in designing strategies to control it. Aggregation is involved in tumor proliferation, amyloid-related diseases (such as Parkinson’s and Alzheimer’s diseases) and pathogen infection. Of the many diverse methods to study aggregation, fluorescence offers exceptional speed and ease. Steady-state fluorescence is more common than time-resolved fluorescence owing to long acquisition times associated with the latter. Our innovative approach, referred to as direct waveform recording, is capable of acquiring high quality time-resolved data at steady-state speeds. The work presented here demonstrates the applicability of this measurement in the study of complex aggregate formation with glycodendrimers.en_US
dc.language.isoen_USen_US
dc.titleAggregation Characterization of Lectin Interactions with Sugar-Functionalized Dendrimersen_US
dc.typePresentationen_US
mus.citation.conferenceMSU Student Research Celebration 2012
mus.relation.collegeCollege of Letters & Science
mus.relation.departmentChemistry & Biochemistry.en_US
mus.relation.universityMontana State University - Bozemanen_US


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