{"database":"GNPS","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://massive-ftp.ucsd.edu/v06/MSV000093497/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Metabolomics"],"submitter":["Wilton Ricardo Sala-Carvalho"],"instrument_platform":["HPLC-MS ESI low resolution (Thermo-Fischer)"],"species":["Brittonodoxa Subpinnata"],"full_dataset_link":["https://massive.ucsd.edu/ProteoSAFe/dataset.jsp?task=fa46caae090741f2b7b48fe508005e1e"],"submitter_email":["wiltonsala@hotmail.com"],"submitter_affiliation":["Universidade de Sao Paulo"],"sample_protocol":[""],"repository":["GNPS"],"file_size":["77"],"ptm_modification":["MS:1002864 - No post-translational-modifications are included in the identified peptides of this dataset"],"data_protocol":[""],"additional_accession":[]},"is_claimable":false,"name":"GNPS - Brittonodoxa subpinnata soluble extract","description":"For HPLC-MS2 analysis, 50 mg of plant material was extracted with 5 mL of 80% methanol. The supernatant was collected and submitted to a cleanup process through a C18 SPE by activating the column with methanol and equilibrating it with ultrapure water. The extract was loaded into the column and eluted with 5 mL of the following solvents: ultrapure water, followed by 25% methanol, 50% methanol, and washed with methanol. The fractions were joined, transferred to a tube, and vacuum dried.","dates":{"publication":"Sat Nov 25 14:04:00 GMT 2023"},"accession":"MSV000093497","cross_references":{"TAXONOMY":["663595"]}}