<HashMap><database>GNPS</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://massive-ftp.ucsd.edu/v07/MSV000094531/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Metabolomics</omics_type><submitter>Mohamed MEHIRI</submitter><instrument_platform>Q Exactive</instrument_platform><species>Dysidea Avara</species><species>Olea Europaea Subsp. Europaea (ncbitaxon:158383)</species><full_dataset_link>https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=2cae78df549147e1bfb64c61c5d1c415</full_dataset_link><submitter_email>Mohamed.MEHIRI@univ-cotedazur.fr</submitter_email><submitter_affiliation>University Cote d Azur</submitter_affiliation><sample_protocol></sample_protocol><repository>GNPS</repository><file_size>9</file_size><ptm_modification>MS:1002864 - No post-translational-modifications are included in the identified peptides of this dataset</ptm_modification><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>GNPS 2404_Workshop_Dysidea_avaria_and_Olea_europa</name><description>Mass spectrometry method: the extracts were analyzed by high-performance liquid chromatography (LC) coupled to a high-resolution tandem mass spectrometer (HRMS, q-Exactive, Orbitrap) fitted with a heated ElectroSpray Ionization (ESI) and operating in positive ionization mode. Fragmentation spectra (MS/MS) were collected in data-dependent mode.
The chromatography conditions were as follow: reverse-phase column (2 um C18 particles, 150 x 2.1 mm) and the mobile phase consisted of acetonitrile-water + 0.1% formic acid (gradient mode starting from 10% acetonitrile to 100% in 30 min). </description><dates><publication>Sat Apr 13 05:21:00 BST 2024</publication></dates><accession>MSV000094531</accession><cross_references/></HashMap>