<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><submitter/><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BIAD1326</full_dataset_link><repository>bioimages</repository><figure_sub>Specimen</figure_sub><figure_sub>Funding</figure_sub><figure_sub>Study Component</figure_sub><figure_sub>organisation</figure_sub><figure_sub>Biosample</figure_sub><figure_sub>Associations</figure_sub><figure_sub>Image acquisition</figure_sub><pubmed_authors>Rainer Kurmayer</pubmed_authors><pubmed_authors>Rubén Morón Asensio</pubmed_authors></additional><is_claimable>false</is_claimable><name>Subcellular  visualization and quantification of cyanotoxins microcystin or anabaenopeptin synthesis in bloom-forming cyanobacteria shows a distinct compartmentation</name><description>In this study time-lapse experiments have been performed using pulsed feeding of non-natural amino acids (non-AAs) in order to observe the build up or decline of azide- or alkyne-modified (clickable) microcystins (MCs) or anabaenopetins (APs) in M. aeruginosa and P. agardhii. Clickable MCs or APs have been subsequently labeled via Copper-catalyzed Azide-Alkyne Cycloaddition (CuAAC) with ALEXA Fluor 488 (A488) and visualized using confocal microscopy and advanced image analysis using Imaris 10.1 surfaces function</description><dates><release>2024-11-29T00:00:00Z</release><modification>2026-01-06T09:22:46.403Z</modification><creation>2024-08-16T16:18:43.745Z</creation></dates><accession>S-BIAD1326</accession><cross_references/></HashMap>