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MB Sample ID: SA100890

Local Sample ID:mouse_2
Subject ID:SU001453
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6
Age Or Age Range:postnatal day 56
Gender:Male
Animal Housing:Cage Type: Innovive, Catalog#M-BTM, San Diego, CA; Bedding Type: cellulose fiber chips;
Animal Light Cycle:12:12
Animal Feed:22/5 Rodent Diet
Animal Water:Aquavive, Catalog#M-WB-300A, INNOVIVE, San Diego, CA

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Subject:

Subject ID:SU001453
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090
Genotype Strain:C57BL/6
Age Or Age Range:postnatal day 56
Gender:Male
Animal Housing:Cage Type: Innovive, Catalog#M-BTM, San Diego, CA; Bedding Type: cellulose fiber chips;
Animal Light Cycle:12:12
Animal Feed:22/5 Rodent Diet
Animal Water:Aquavive, Catalog#M-WB-300A, INNOVIVE, San Diego, CA

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
mouse_2SA100890FL014193vehicleTCDD treatment(ug/kg)

Collection:

Collection ID:CO001448
Collection Summary:Mice were taken down with CO2. Livers were excised and immediately frozen in liquid nitrogen.
Collection Protocol Comments:Time-point: 28; Time-point Unit: DAYS;
Sample Type:Liver

Treatment:

Treatment ID:TR001468
Treatment Summary:oral gavage every 4 days for 28 days. 7 total exposures with sesame oil vehicle or 0.3-30 ug/kg TCDD.
Treatment Protocol Comments:Administration Interval: 4; Administration Interval Unit: DAYS; Dose Unit: ug/kg; Number of Administrations: 7; Chemical Soucre: AccuStandard; Chemical Catalog Number: S-70982; Chemical Purity: -; Vehicle Substance: CHEBI 28119
Treatment Compound:2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)
Treatment Route:GAVAGE
Treatment Dose:0.3,1,3,10,30
Treatment Dosevolume:0.1 ml
Treatment Vehicle:Sesame oil
Animal Fasting:2 hrs before end-point
Animal Endp Euthanasia:CO2

Sample Preparation:

Sampleprep ID:SP001461
Sampleprep Summary:Frozen liver tissue was homegenized in 4.6 ml h20:methanol (5:3) mixture and homegenized, 2.9 ml chloroform was added,vortexed and spun down at 5,000G. Top layer was removed and blown down with nitrogen and reconstituted in 400 l 10mM tetrabutylammonium (TBA)+10mM acetate (pH 5). A further 1:16 dilution was performed for analysis of acetyl-CoA. Coenzyme A (CoA) was measured by standard addition method by diluting with TBA containing CoA standard resulting in 1 uM CoA standard addition. 1 uM CoA standard addition samples are denoted in the subject sample factor section.
Processing Method:Liquid extraction
Processing Storage Conditions:-80℃

Combined analysis:

Analysis ID AN002299
Analysis type MS
Chromatography type Reversed phase
Chromatography system Waters Acquity
Column Waters Ascentis Express C18 (2.1 x 5 cm)
MS Type ESI
MS instrument type TOF
MS instrument name Waters Xevo G2 XS QTof
Ion Mode NEGATIVE
Units normalized signal area

Chromatography:

Chromatography ID:CH001689
Instrument Name:Waters Acquity
Column Name:Waters Ascentis Express C18 (2.1 x 5 cm)
Chromatography Type:Reversed phase

MS:

MS ID:MS002142
Analysis ID:AN002299
Instrument Name:Waters Xevo G2 XS QTof
Instrument Type:TOF
MS Type:ESI
MS Comments:Samples were run in MS^e mode. MassLynx V4.2 was used to measure area under the curve. Accurate mass and retention were used for identification of signal for respective metabolites.
Ion Mode:NEGATIVE
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