<HashMap><database>MetaboLights</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/m_MTBLS15334_LC-MS_negative_reverse-phase_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/i_Investigation.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/s_MTBLS15334.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/a_MTBLS15334_LC-MS_negative_reverse-phase.txt</Txt><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA3.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl4.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS4.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl2.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS2.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA5.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl5.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl3.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA2.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS5.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA1.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS1.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA4.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS3.zip</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl1.zip</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><ftp_download_link>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334</ftp_download_link><metabolite_identification_protocol>&lt;p>After analyzing all the target substances' chromatographic peaks, the integrals were calculated. A standard curve was constructed using the standards to perform quantitative analysis, and the on-machine detection concentration was obtained. Further, based on the sample sampling volume, the specific content data of the target substances in the samples were calculated.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - negative - reverse-phase</instrument_platform><chromatography_protocol>&lt;p>Using a Kinetex C8 chromatographic column (100Å, 2.6 µm, 2.1 mm × 100 mm), with a flow rate of 0.3 mL/min, column temperature of 40 ℃, auto sampler at 4 ℃, and injection volume of 1 μL. The mobile phase A is 0.1% formic acid water, and the mobile phase B is 50% methanol-isopropanol (containing 0.1% formic acid). The gradient of the mobile phase is as follows: 0-1 min: A/B is 80:20 (V/V); 6&lt;/p>&lt;p>Min: A/B ratio is 60:40 (volume/volume); for 9-10 minutes, the ratio becomes 80:20 (volume/volume).&lt;/p></chromatography_protocol><publication>Targeted metabolomics of mouse feces with sodium propionate supplementation.</publication><submitter_name>jiang fei</submitter_name><submitter_affiliation>Xiangya Hospital, Central South University</submitter_affiliation><organism_part>feces</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>The entire experiment was conducted on ice.&lt;/p>&lt;p>2. Take 20 mg of solid sample and add it to a 2 mL centrifuge tube. Add two steel balls and 800 μL of extraction agent (containing an internal standard). Vortex for 60 seconds.&lt;/p>&lt;p>3. Put it in the tissue grinder and grind at 55 Hz for 60 seconds.&lt;/p>&lt;p>4. Repeat this once.&lt;/p>&lt;p>5. Centrifuge at 4000g for 10 minutes at 10°C.&lt;/p>&lt;p>6. Take 40 μL of the supernatant, add 20 μL of 200 mM 3-NPH and mix well.&lt;/p>&lt;p>7. Add 20 μL of 120 mM (EDC)·HCl-6% pyridine solution and mix well.&lt;/p>&lt;p>8. In a constant temperature metal shaker at 40°C, vibrate at 1200 rpm for 30 minutes.&lt;/p>&lt;p>9. After the reaction, place it on ice to cool for 3 minutes.&lt;/p>&lt;p>10. Centrifuge at 12000g for 10 minutes at 4°C.&lt;/p>&lt;p>11. Take the supernatant, add 150 μL of 0.1% formic acid water (v/v) to make up to 200 μL, vortex and mix well for 60 seconds.&lt;/p>&lt;p>12. Centrifuge at 12000g for 10 minutes at 4°C.&lt;/p>&lt;p>13. Take the supernatant, pass it through a 0.22 μm filter membrane. Transfer the filtrate to a bottle, with the volume of the bottle not less than 50 μL per bottle.&lt;/p></extraction_protocol><organism>Mus nusculus</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS15334</full_dataset_link><author>jiang fei. Xiangya Hospital, Central South University. feijiangfj@csu.edu.cn.</author><data_transformation_protocol>&lt;p>The data were processed using the quantitative software OS (version: 4.7, SCIEX) to obtain the mass spectrometry analysis data of different samples. &lt;/p></data_transformation_protocol><study_factor>Sodium propionate</study_factor><submitter_email>feijiangfj@csu.edu.cn</submitter_email><sample_collection_protocol>&lt;p>mouse feces. ctrl, ps, sodium propiionate.&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Mus nusculus</study_design><study_design>Metabolomics</study_design><study_design>ProteoWizard msconvert</study_design><study_design>AB SCIEX Triple Quad 6500+</study_design><study_design>colorectal cancer</study_design><study_design>targeted analysis</study_design><study_design>experimental blank</study_design><study_design>SCIEX</study_design><study_design>AB SCIEX</study_design><study_design>feces</study_design><curator_keywords>Mus nusculus</curator_keywords><curator_keywords>Metabolomics</curator_keywords><curator_keywords>ProteoWizard msconvert</curator_keywords><curator_keywords>AB SCIEX Triple Quad 6500+</curator_keywords><curator_keywords>colorectal cancer</curator_keywords><curator_keywords>targeted analysis</curator_keywords><curator_keywords>experimental blank</curator_keywords><curator_keywords>SCIEX</curator_keywords><curator_keywords>AB SCIEX</curator_keywords><curator_keywords>feces</curator_keywords><mass_spectrometry_protocol>&lt;p>The SCIEX Citrine Triple Quad TM mass spectrometer uses the software OS (version: 4.7, SCIEX), and operates in the negative ESI (Electrospray Ionization) mode, employing the multiple reaction monitoring (MRM) data acquisition method. Ion source parameters: the negative mode voltage of the ion spray (Ionspray, IS) is -4500V, the spray gas (GS1) and auxiliary heating gas (GS2) are 50psi and 50 psi respectively, and the desolvation gas temperature is 550℃; the gas curtain gas (Curtain Gas, CUR) is 30 psi, and the collision gas (Collision Gas, CAD) is 10.&lt;/p></mass_spectrometry_protocol></additional><is_claimable>false</is_claimable><name>Targeted metabolomics of mouse feces with sodium propionate supplementation</name><description>Targeted metabolomics of mouse feces with sodium propionate supplementation</description><dates><publication>2027-08-13</publication><submission>2026-08-13</submission></dates><accession>MTBLS15334</accession><cross_references/></HashMap>