Return to study ST003114 main page

MB Sample ID: SA337381

Local Sample ID:S16_mitos_linoleic.acid_KO_4
Subject ID:SU003230
Subject Type:Cultured cells
Subject Species:Homo sapiens
Taxonomy ID:9606

Select appropriate tab below to view additional metadata details:


Combined analysis:

Analysis ID AN005102 AN005103 AN005104 AN005105
Analysis type MS MS MS MS
Chromatography type None (Direct infusion) Normal phase Reversed phase Reversed phase
Chromatography system Advion TriVersa NanoMate Agilent 1260 Shimadzu Nexera X2 Shimadzu Nexera X2
Column None Macherey-Nagel Nucleosil NH2 (50×2 mm, 3 um, 120 Å) Waters Acquity BEH Shield RP18 (100×2.1 mm, 1.7 um) Phenomenex Core-Shell Kinetex Biphenyl (100×3.0 mm, 2.6 um, 100 Å)
MS Type ESI ESI ESI ESI
MS instrument type QTRAP QTRAP QTRAP QTRAP
MS instrument name SCIEX QTRAP 6500 SCIEX QTRAP 6500 SCIEX QTRAP 6500 SCIEX QTRAP 6500
Ion Mode POSITIVE POSITIVE POSITIVE NEGATIVE
Units counts per second (cps) counts per second (cps) counts per second (cps) counts per second (cps)

MS:

MS ID:MS004839
Analysis ID:AN005102
Instrument Name:SCIEX QTRAP 6500
Instrument Type:QTRAP
MS Type:ESI
MS Comments:PC, PE, PI, PS, PG, and PA species were analyzed by Nano-Electrospray Ionization Tandem Spectrometry (Nano-ESI-MS/MS) with direct infusion of the lipid extract (Shotgun Lipidomics) as previously described (Kumar et al., J Cell Biol 2015, 211, 1057).
Ion Mode:POSITIVE
  
MS ID:MS004840
Analysis ID:AN005103
Instrument Name:SCIEX QTRAP 6500
Instrument Type:QTRAP
MS Type:ESI
MS Comments:LC-ESI-MS/MS analysis of ceramides and sphingomyelins was conducted as previously published (Oteng et al., J Lipid Res 2017, 58, 1100; Schwamb et al., Blood 2012, 120, 3978).
Ion Mode:POSITIVE
  
MS ID:MS004841
Analysis ID:AN005104
Instrument Name:SCIEX QTRAP 6500
Instrument Type:QTRAP
MS Type:ESI
MS Comments:Cardiolipin (CL) species were analyzed by Liquid Chromatography coupled to Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS). CL species were monitored in the positive ion mode using the following Multiple Reaction Monitoring (MRM) transitions: CL 68:4, m/z 1418.9 to 575.4; CL 70:4, m/z 1446.9 to 575.4; CL 72:4 m/z 1475.0 to 603.4; CL 61:1 (internal standard), m/z 1326.9 to 535.4. For all MRM transitions the values for declustering potential, entrance potential, collision energy, and cell exit potential were 140 V, 10 V, 45 V, and 7 V, respectively (Tatsuta, Methods Mol Biol 2017, 1567, 79). The instrument settings for nebulizer gas (Gas 1), turbo gas (Gas 2), curtain gas, and collision gas were 50 psi, 50 psi, 40 psi, and medium, respectively. The Turbo V ESI source temperature was 500 °C, and the ionspray voltage was 4.5 kV. The LC chromatogram peaks of the endogenous CL species and the internal standard CL 61:1 were integrated using the MultiQuant 3.0.2 software (SCIEX).
Ion Mode:POSITIVE
  
MS ID:MS004842
Analysis ID:AN005105
Instrument Name:SCIEX QTRAP 6500
Instrument Type:QTRAP
MS Type:ESI
MS Comments:Fatty acid levels were determined by LC-ESI-MS/MS: Fatty acids were monitored in the negative ion mode using “pseudo” Multiple Reaction Monitoring (MRM) transitions (Hellmuth et al., Anal Chem 2012, 84, 1483). The instrument settings for nebulizer gas (Gas 1), turbo gas (Gas 2), curtain gas, and collision gas were 60 psi, 90 psi, 40 psi, and medium, respectively. The Turbo V ESI source temperature was 650 °C, and the ionspray voltage was -4 kV. The LC chromatogram peaks of the endogenous fatty acids and the internal standard palmitic-d31 acid were integrated using the MultiQuant 3.0.2 software (SCIEX).
Ion Mode:NEGATIVE
  logo