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MB Sample ID: SA343209

Local Sample ID:Mul1(-/-)_TZ 39
Subject ID:SU003294
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:Wild type and Mul1(+/+) mice
Age Or Age Range:8 weeks
Gender:Male and female
Animal Light Cycle:12-hour/12-hour light/dark cycle
Animal Feed:Research Diets D12492

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Subject:

Subject ID:SU003294
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:Wild type and Mul1(+/+) mice
Age Or Age Range:8 weeks
Gender:Male and female
Animal Light Cycle:12-hour/12-hour light/dark cycle
Animal Feed:Research Diets D12492

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
Mul1(-/-)_TZ 39SA343209FL040569Mul1(-/-) Genotype
Mul1(-/-)_TZ 39SA343209FL040569LiverSample source

Collection:

Collection ID:CO003287
Collection Summary:Liver tissue was obtained from Mul1(+/+) and Mul1(-/-) mice following a HFD for 16 weeks and stained with H&E or Oil Red Oil.
Sample Type:Liver
Storage Conditions:-20℃

Treatment:

Treatment ID:TR003303
Treatment Summary:Liver tissue was obtained from Mul1(+/+) and Mul1(-/-) mice following a HFD for 16 weeks and stained with H&E or Oil Red Oil.

Sample Preparation:

Sampleprep ID:SP003301
Sampleprep Summary:liver tissues from mice were fixed overnight in 10% neutral formalin and embedded in paraffin. Paraffin-embedded tissues were cut into sections and stained with hematoxylin and eosin (H&E) for assessment of liver histology. Liver tissue from Mul1(+/+) and Mul1(-/-) mice on HFD were subjected to the Folch extraction in order to separate lipids and polar metabolites.
Processing Storage Conditions:4℃
Extract Storage:-20℃

Combined analysis:

Analysis ID AN005211 AN005212
Analysis type MS MS
Chromatography type Reversed phase Reversed phase
Chromatography system Thermo Dionex Ultimate 3000 Thermo Dionex Ultimate 3000
Column Waters ACQUITY UPLC BEH C18 (100 x 2.1mm,1.7um) Waters ACQUITY UPLC BEH C18 (100 x 2.1mm,1.7um)
MS Type ESI ESI
MS instrument type Orbitrap Orbitrap
MS instrument name Thermo Q Exactive Orbitrap Thermo Q Exactive Orbitrap
Ion Mode POSITIVE NEGATIVE
Units A.U. A.U.

Chromatography:

Chromatography ID:CH003942
Instrument Name:Thermo Dionex Ultimate 3000
Column Name:Waters ACQUITY UPLC BEH C18 (100 x 2.1mm,1.7um)
Column Temperature:50
Flow Gradient:0−0.5 min, 60% B; 0.5−2 min, 60−95% B; 2−17 min, 95% B; 17−17.5 min, 95−60% B; 17.5−20 min, 60% B
Flow Rate:350 µl/min
Solvent A:60:40 acetonitrile:water; 10mM ammonium formate; 0.1% formic acid
Solvent B:90:8:2 2-propanol:acetonitrile:water; 10mM ammonium formate; 0.1% formic acid
Chromatography Type:Reversed phase

MS:

MS ID:MS004944
Analysis ID:AN005211
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:The aqueous phase was analyzed using the Thermo Q-Exactive Orbitrap mass spectrometer with Dionex UHPLC and autosampler. All samples were analyzed in positive and negative simultaneously with heated electrospray ionization (HESI) with a mass resolution of 35,000 at m/z 200 as separate injections. The polar metabolites were analyzed on Thermo Q-Exactive Orbitrap mass spectrometer equipped with UHPLC. Data were analyzed with MZmine and features were aligned for identification across samples. The metabolites were searched against the Southeastern Center for Integrated Metabolomics (SECIM) metabolite library using retention time and corresponding mass spectral data. Lipids isolated from Folch extraction procedure were also analyzed by the same instrument. Lipidomics data were analyzed using the LipidMatch software and identified lipid entities were exported in a tabular form.
Ion Mode:POSITIVE
  
MS ID:MS004945
Analysis ID:AN005212
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:The aqueous phase was analyzed using the Thermo Q-Exactive Orbitrap mass spectrometer with Dionex UHPLC and autosampler. All samples were analyzed in positive and negative simultaneously with heated electrospray ionization (HESI) with a mass resolution of 35,000 at m/z 200 as separate injections. The polar metabolites were analyzed on Thermo Q-Exactive Orbitrap mass spectrometer equipped with UHPLC. Data were analyzed with MZmine and features were aligned for identification across samples. The metabolites were searched against the Southeastern Center for Integrated Metabolomics (SECIM) metabolite library using retention time and corresponding mass spectral data. Lipids isolated from Folch extraction procedure were also analyzed by the same instrument. Lipidomics data were analyzed using the LipidMatch software and identified lipid entities were exported in a tabular form.
Ion Mode:NEGATIVE
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