Summary of Study ST003142

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 PR001953. The data can be accessed directly via it's Project DOI: 10.21228/M88M77 This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003142
Study TitleEffect of liver Acox1 knockout on serum lipidome in mice
Study SummaryThe liver gene expression of the peroxisomal β-oxidation enzyme acyl-coenzyme A oxidase 1 (ACOX1), which catabolizes very long chain fatty acids (VLCFA), increases in the context of obesity. To check if liver peroxisomal fatty acids beta-oxidation deficiency will affect whole body metabolic homeostasis through circulating lipids. We analyzed serum samples from 5 WT and 5 Acox1-LKO mice.
Institute
Washington University in St. Louis
Last NameLu
First NameDongliang
Address660 S. Euclid Ave.
Emailludong-liang@wustl.edu
Phone3147476766
Submit Date2024-03-19
Analysis Type DetailLC-MS
Release Date2024-03-27
Release Version1
Dongliang Lu Dongliang Lu
https://dx.doi.org/10.21228/M88M77
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Combined analysis:

Analysis ID AN005155 AN005156
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000
Column Waters ACQUITY UPLC CSH C18 (100 x 2.1mm,1.7um) Waters ACQUITY UPLC CSH C18 (100 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type QTOF QTOF
MS instrument name Bruker Impact HD Bruker Impact HD
Ion Mode POSITIVE NEGATIVE
Units peak area peak area

MS:

MS ID:MS004891
Analysis ID:AN005155
Instrument Name:Bruker Impact HD
Instrument Type:QTOF
MS Type:ESI
MS Comments:The acquisition rate was 1.44 Hz for MS acquisition and 4 – 10 Hz for MS/MS spectra acquisition, with an m/z range from 150 to 1500. For both positive and negative ionization. Intensity threshold:2500 cts for positive ionization. Lipid features were extracted and aligned using software LipidScreener 1.1.0
Ion Mode:POSITIVE
Capillary Voltage:4200 V
Collision Energy:10-70 eV
Dry Gas Flow:5.0 L/min
Dry Gas Temp:240°C
Nebulizer:1.2 Bar
  
MS ID:MS004892
Analysis ID:AN005156
Instrument Name:Bruker Impact HD
Instrument Type:QTOF
MS Type:ESI
MS Comments:The acquisition rate was 1.44 Hz for MS acquisition and 4 – 10 Hz for MS/MS spectra acquisition, with an m/z range from 150 to 1500. For both positive and negative ionization. Intensity threshold:1500 cts for negative ionization. Lipid features were extracted and aligned using software LipidScreener 1.1.0
Ion Mode:NEGATIVE
Capillary Voltage:4200 V
Collision Energy:10-70 eV
Dry Gas Flow:5.0 L/min
Dry Gas Temp:240°C
Nebulizer:1.2 Bar
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