<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>53(3)</volume><submitter>Dodes Traian MM</submitter><pubmed_abstract>Lateral organization of biological membranes is frequently studied using fluorescence microscopy. One of the most widely used probes for these studies is 2-dimethylamino-6-lauroylnaphthalene (laurdan). The fluorescence of this probe is sensitive to the environment polarity, and thus laurdan reports the local penetration of water when inserted in membranes. Unfortunately, this probe can only be used under two-photon excitation due to its low photostability. This is a very important limitation, because there are not too many laboratories with capability for two-photon microscopy. In this work, we explored the performance of 6-dodecanoyl-2-[N-methyl-N-(carboxymethyl)amino]naphthalene (C-laurdan), a carboxyl-modified version of laurdan, for imaging biological membranes using a conventional con</pubmed_abstract><journal>Journal of lipid research</journal><pagination>609-616</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3276485</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Imaging lipid lateral organization in membranes with C-laurdan in a confocal microscope.</pubmed_title><pmcid>PMC3276485</pmcid><pubmed_authors>Levi V</pubmed_authors><pubmed_authors>Dodes Traian MM</pubmed_authors><pubmed_authors>Flecha FLG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Imaging lipid lateral organization in membranes with C-laurdan in a confocal microscope.</name><description>Lateral organization of biological membranes is frequently studied using fluorescence microscopy. One of the most widely used probes for these studies is 2-dimethylamino-6-lauroylnaphthalene (laurdan). The fluorescence of this probe is sensitive to the environment polarity, and thus laurdan reports the local penetration of water when inserted in membranes. Unfortunately, this probe can only be used under two-photon excitation due to its low photostability. This is a very important limitation, because there are not too many laboratories with capability for two-photon microscopy. In this work, we explored the performance of 6-dodecanoyl-2-[N-methyl-N-(carboxymethyl)amino]naphthalene (C-laurdan), a carboxyl-modified version of laurdan, for imaging biological membranes using a conventional con</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Mar</publication><modification>2025-04-26T07:40:42.334Z</modification><creation>2019-03-27T00:48:58Z</creation></dates><accession>S-EPMC3276485</accession><cross_references><pubmed>22184757</pubmed><doi>10.1194/jlr.d021311</doi><doi>10.1194/jlr.D021311</doi></cross_references></HashMap>