Summary of Study ST001439

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR000989. The data can be accessed directly via it's Project DOI: 10.21228/M8VH7G This work is supported by NIH grant, U2C- DK119886.

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Study IDST001439
Study TitleMetabolites in contents of small intestine in wild type and DAOG181R/G181R mice
Study SummaryTo investigate if DAO regulates metabolites in intestinal lumen, we compared metabolites in contents of small intestine in wild type and DAOG181R/G181R mice. All mice have C57BL/6 background and 8 weeks of age.
Institute
Keio University
DepartmentPharmacology
Last NameSuzuki
First NameMasataka
Address35, Shinanomachi, Shinjuku-ku, Tokyo
Emailmasataka.s@keio.jp
Phone+81-3-5363-3750
Submit Date2019-12-17
Analysis Type DetailMS
Release Date2020-08-04
Release Version1
Masataka Suzuki Masataka Suzuki
https://dx.doi.org/10.21228/M8VH7G
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN002403 AN002404
Analysis type MS MS
Chromatography type None (Direct infusion) None (Direct infusion)
Chromatography system none none
Column none none
MS Type ESI ESI
MS instrument type QTOF QTOF
MS instrument name Agilent 6210 TOF Agilent 6230 TOF
Ion Mode UNSPECIFIED UNSPECIFIED
Units relative_area relative_area

MS:

MS ID:MS002244
Analysis ID:AN002403
Instrument Name:Agilent 6210 TOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:System control: Agilent G2201AA ChemStation software version B .03.01 Peaks were extracted using automatic integration software MasterHands to obtain peal information including m/z, peak area and migration time. Detected metabolites were plotted on metabolic pathway maps using VANTED software.
Ion Mode:UNSPECIFIED
  
MS ID:MS002245
Analysis ID:AN002404
Instrument Name:Agilent 6230 TOF
Instrument Type:QTOF
MS Type:ESI
MS Comments:System control: Agilent G2201AA ChemStation software version B .03.01 Peaks were extracted using automatic integration software MasterHands to obtain peal information including m/z, peak area and retention time. Detected metabolites were plotted on metabolic pathway maps using VANTED software.
Ion Mode:UNSPECIFIED
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