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MB Sample ID: SA177707

Local Sample ID:KO_ZT22_1
Subject ID:SU001993
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

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Subject:

Subject ID:SU001993
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
KO_ZT22_1SA177707FL021968KO_ZT22Group
KO_ZT22_1SA177707FL021968Rev-erb cardiomyocyte specific knock outGenotype
KO_ZT22_1SA177707FL021968KO mouse heart ventrcle harvest at ZT22Experimental variables

Collection:

Collection ID:CO001986
Collection Summary:Snap-frozen heart ventricles were collected from both WT and Rev-erb cardiomyocyte-specific KO mice at ZT10 or ZT22
Sample Type:Heart

Treatment:

Treatment ID:TR002005
Treatment Summary:no special treatment

Sample Preparation:

Sampleprep ID:SP001999
Sampleprep Summary:Heart ventricle tissues were harvested from male mice at 3 months old (n = 3 at each condition) and were snap-frozen in liquid nitrogen. Lipids were extracted as previously described 55–57. Lipids were separated on a Shimadzu CTO-20A Nexera X2 UHPLC systems, 1.8 μm particle 50 × 2.1 mm Acquity HSS UPLC T3 column (Waters, Milford, MA). Lipidomics acquisition performed in both pos and neg mode ionization. Pos mode lipids were normalized by Internal Standard PC 17:0; [M+H]+, Neg mode lipids were normalized by Internal Standard PC 34:0.

Combined analysis:

Analysis ID AN003113
Analysis type MS
Chromatography type GC
Chromatography system Shimadzu Nexera X2
Column Waters Acquity BEH HSS T3 (100 x 2.1mm,1.8um)
MS Type EI
MS instrument type Other
MS instrument name Shimadzu QP2010 Plus
Ion Mode UNSPECIFIED
Units pmoles/l

Chromatography:

Chromatography ID:CH002298
Instrument Name:Shimadzu Nexera X2
Column Name:Waters Acquity BEH HSS T3 (100 x 2.1mm,1.8um)
Chromatography Type:GC

MS:

MS ID:MS002894
Analysis ID:AN003113
Instrument Name:Shimadzu QP2010 Plus
Instrument Type:Other
MS Type:EI
MS Comments:Statistical analyses were performed with either ANOVA or t-test in R Studio (R Studio Inc., Boston, MA). Differential metabolites were identified by adjusting the p-values for multiple testing at an FDR (Benjamini Hochberg method) threshold of <0.25.
Ion Mode:UNSPECIFIED
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