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MB Sample ID: SA338016

Local Sample ID:C92DG_07
Subject ID:SU003234
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

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Subject:

Subject ID:SU003234
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
C92DG_07SA338016FL040037BrainSample source
C92DG_07SA338016FL040037C9orf72Genotype
C92DG_07SA338016FL0400372DGTreatment

Collection:

Collection ID:CO003227
Collection Summary:Animals were euthanized by CO2 inhalation 16 hours following the final injection and transcardially perfused with ice-cold PBS. Whole brains and spinal cords were then excised, flash frozen in liquid N2, and stored at –80°C
Sample Type:Brain cortex

Treatment:

Treatment ID:TR003243
Treatment Summary:Animals were administered i.p. injections of saline or 4 g/kg 2DG twice weekly for six weeks

Sample Preparation:

Sampleprep ID:SP003241
Sampleprep Summary:Metabolites from equal amounts of frontal cortex tissue were rapidly extracted in 80% ice-cold methanol. Extracted samples were vortexed twice, cleared by centrifugation at 14,000 x g for 20 minutes at 4°C, and stored at -80°C.

Combined analysis:

Analysis ID AN005111
Analysis type MS
Chromatography type HILIC
Chromatography system Thermo Vanquish
Column Merck SeQuant ZIC-pHILIC (150 x 2.1mm,5um)
MS Type ESI
MS instrument type Orbitrap
MS instrument name Thermo Q Exactive Orbitrap
Ion Mode UNSPECIFIED
Units peak intensity

Chromatography:

Chromatography ID:CH003867
Instrument Name:Thermo Vanquish
Column Name:Merck SeQuant ZIC-pHILIC (150 x 2.1mm,5um)
Column Temperature:30
Flow Gradient:85% to 30% A in 20 min followed by a wash with 30% A and re-equilibration at 85% A
Flow Rate:150 μL/min
Solvent A:100% acetonitrile
Solvent B:100% water; 0.1% ammonium hydroxide; 20 mM ammonium acetate
Chromatography Type:HILIC

MS:

MS ID:MS004848
Analysis ID:AN005111
Instrument Name:Thermo Q Exactive Orbitrap
Instrument Type:Orbitrap
MS Type:ESI
MS Comments:A Sequant ZIC-pHILIC column (2.1 mm i.d. × 150 mm, particle size of 5 µm, Millipore Sigma) was used for separation of metabolites. A 2.1 × 20 mm guard column with the same packing material was used for protection of the analytical column. Flow rate was set at 150 μL/min. Buffers consisted of 100% acetonitrile for mobile phase A, and 0.1% NH4OH/20 mM CH3COONH4 in water for mobile phase B. The chromatographic gradient ran from 85% to 30% A in 20 min followed by a wash with 30% A and re-equilibration at 85% A. Column temperature was 30 C.
Ion Mode:UNSPECIFIED
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