<HashMap><database>bioimages</database><scores/><additional><omics_type>Unknown</omics_type><volume>154</volume><volume>7</volume><submitter>Mike Heilemann</submitter><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BSST712</full_dataset_link><repository>bioimages</repository><figure_sub>Organization</figure_sub><pubmed_authors>Mike Heilemann</pubmed_authors><pubmed_authors>Marina S Dietz</pubmed_authors><pubmed_authors>Johanna V Rahm</pubmed_authors><pubmed_authors>Marie-Lena IE Harwardt</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-particle tracking (SPT) data of MET with a non-activating Fab ligand and the activating ligand InlB321 recorded in HeLa cells</name><description>Universal point accumulation for imaging in nanoscale topography (uPAINT) was applied to measure the dynamics of the MET receptor in living HeLa cells. For the resting receptor, an ATTO 647N-labeled, non-activating Fab antibody fragment was used. The ligand-bound state was probed using the InlB321 ligand site-specifically labeled with ATTO 647N which was fully functional. Imaging was performed in total internal reflection fluorescence (TIRF) mode using an N-STORM microscope (Nikon, Japan).</description><dates><release>2021-09-23T00:00:00Z</release><modification>2023-04-19T13:54:42.663Z</modification><creation>2021-09-23T17:19:56Z</creation></dates><accession>S-BSST712</accession><cross_references/></HashMap>