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MB Sample ID: SA154461

Local Sample ID:CTRL_2
Subject ID:SU001749
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606

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Subject:

Subject ID:SU001749
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
CTRL_2SA154461FL018155no treatmentTreatment

Collection:

Collection ID:CO001742
Collection Summary:Cells were washed with ice cold PBS and draped
Sample Type:Fibroblasts

Treatment:

Treatment ID:TR001762
Treatment Summary:Cells were either infected adenoviruses encoding GOLPH3 or treated with siRNAs targeting GOLPH3 expression

Sample Preparation:

Sampleprep ID:SP001755
Sampleprep Summary:Samples were fortified with an Internal standard Mix and lipids were extracted twice with an extraction mix consisting of 85:15 Ethyl acetate 70% Isopropanol. All lipids that were used in the Internal standard mix and in the Calibration mixes were purchased from Avanti Polar Lipids Inc. After evaporating the cell extract to dryness, the samples were reconstituted in the mobile phase.

Combined analysis:

Analysis ID AN002730
Analysis type MS
Chromatography type Reversed phase
Chromatography system Thermo Accela 1250
Column Thermo Accucore C18 (100 x 2.1mm,2.6um)
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name Thermo Quantum Ultra
Ion Mode POSITIVE
Units pmol

Chromatography:

Chromatography ID:CH002016
Chromatography Summary:Samples were analyzed with a Quantum Ultra triple quadrupole mass spectrometer connected to an Accela HPLC and Accela autosampler using a solvent gradient. Ceramides identity was achieved through MRM analysis with soft fragmentation. Quantitative analysis is based on calibration curves generated for each ceramide.
Instrument Name:Thermo Accela 1250
Column Name:Thermo Accucore C18 (100 x 2.1mm,2.6um)
Chromatography Type:Reversed phase

MS:

MS ID:MS002527
Analysis ID:AN002730
Instrument Name:Thermo Quantum Ultra
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:Samples were analyzed with a Quantum Ultra triple quadrupole mass spectrometer connected to an Accela HPLC and Accela autosampler using a solvent gradient. Ceramides identity was achieved through MRM analysis with soft fragmentation. Quantitative analysis is based on calibration curves generated for each ceramide. J. Bielawski et al. / Methods 39 (2006) 82–91
Ion Mode:POSITIVE
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