{"database":"MetaboLights","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Tabular":["ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/m_MTBLS15334_LC-MS_negative_reverse-phase_v2_maf.tsv"],"Txt":["ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/i_Investigation.txt","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/s_MTBLS15334.txt","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/a_MTBLS15334_LC-MS_negative_reverse-phase.txt"],"Other":["ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA3.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl4.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS4.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl2.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS2.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA5.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl5.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl3.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA2.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS5.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA1.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS1.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PA4.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/PS3.zip","ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334/FILES/RAW_FILES/Ctrl1.zip"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"ftp_download_link":["ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS15334"],"metabolite_identification_protocol":["<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.</p>"],"repository":["MetaboLights"],"study_status":["Public"],"ptm_modification":[""],"instrument_platform":["Liquid Chromatography MS - negative - reverse-phase"],"chromatography_protocol":["<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</p><p>Min: A/B ratio is 60:40 (volume/volume); for 9-10 minutes, the ratio becomes 80:20 (volume/volume).</p>"],"publication":["Targeted metabolomics of mouse feces with sodium propionate supplementation."],"submitter_name":["jiang fei"],"submitter_affiliation":["Xiangya Hospital, Central South University"],"organism_part":["feces"],"technology_type":["mass spectrometry assay"],"disease":[""],"extraction_protocol":["<p>The entire experiment was conducted on ice.</p><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.</p><p>3. Put it in the tissue grinder and grind at 55 Hz for 60 seconds.</p><p>4. Repeat this once.</p><p>5. Centrifuge at 4000g for 10 minutes at 10°C.</p><p>6. Take 40 μL of the supernatant, add 20 μL of 200 mM 3-NPH and mix well.</p><p>7. Add 20 μL of 120 mM (EDC)·HCl-6% pyridine solution and mix well.</p><p>8. In a constant temperature metal shaker at 40°C, vibrate at 1200 rpm for 30 minutes.</p><p>9. After the reaction, place it on ice to cool for 3 minutes.</p><p>10. Centrifuge at 12000g for 10 minutes at 4°C.</p><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.</p><p>12. Centrifuge at 12000g for 10 minutes at 4°C.</p><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.</p>"],"organism":["Mus nusculus"],"full_dataset_link":["https://www.ebi.ac.uk/metabolights/MTBLS15334"],"author":["jiang fei. Xiangya Hospital, Central South University. feijiangfj@csu.edu.cn."],"data_transformation_protocol":["<p>The data were processed using the quantitative software OS (version: 4.7, SCIEX) to obtain the mass spectrometry analysis data of different samples. </p>"],"study_factor":["Sodium propionate"],"submitter_email":["feijiangfj@csu.edu.cn"],"sample_collection_protocol":["<p>mouse feces. ctrl, ps, sodium propiionate.</p>"],"omics_type":["Metabolomics"],"study_design":["Mus nusculus","Metabolomics","ProteoWizard msconvert","AB SCIEX Triple Quad 6500+","colorectal cancer","targeted analysis","experimental blank","SCIEX","AB SCIEX","feces"],"curator_keywords":["Mus nusculus","Metabolomics","ProteoWizard msconvert","AB SCIEX Triple Quad 6500+","colorectal cancer","targeted analysis","experimental blank","SCIEX","AB SCIEX","feces"],"mass_spectrometry_protocol":["<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.</p>"],"additional_accession":[]},"is_claimable":false,"name":"Targeted metabolomics of mouse feces with sodium propionate supplementation","description":"Targeted metabolomics of mouse feces with sodium propionate supplementation","dates":{"publication":"2027-08-13","submission":"2026-08-13"},"accession":"MTBLS15334","cross_references":{}}