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The present study uses confocal microscopy to identify the localization of carboxyfluorescein\u2010labeled amylin in <jats:styled-content style=\"fixed-case\">RIN<\/jats:styled-content>\u20105<jats:styled-content style=\"fixed-case\">F<\/jats:styled-content> cells. In addition, the size of the aggregates that are formed was evaluated using nanoparticle tracking analysis. In support of previous findings, amylin was observed to interact with and remain associated with the cell membrane. 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