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MB Sample ID: SA114974

Local Sample ID:PL3_HA_44243
Subject ID:SU001482
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

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Combined analysis:

Analysis ID AN002352 AN002353 AN002354
Analysis type MS MS MS
Chromatography type HILIC Reversed phase Reversed phase
Chromatography system Waters Acquity UPLC Waters Acquity UPLC Waters Acquity UPLC
Column Waters Acquity UPLC BEH amide,(100 x 2.1mm,1.7um,100 Å) Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um,100 Å) Waters ACQUITY UPLC HSS T3 (100 x 2.1mm,1.8um,100 Å)
MS Type ESI ESI ESI
MS instrument type QTOF QTOF QTOF
MS instrument name Waters Xevo G2-XS Waters Xevo G2-XS Waters Xevo G2-XS
Ion Mode POSITIVE POSITIVE POSITIVE
Units normalized ion abundance normalized ion abundance normalized ion abundance

MS:

MS ID:MS002194
Analysis ID:AN002352
Instrument Name:Waters Xevo G2-XS
Instrument Type:QTOF
MS Type:ESI
MS Comments:Mass spectrometry data was acquired using ‘sensitivity’ mode in positive and negative electrospray ionization mode within 50-1200 Da range. For the electrospray acquisition, the capillary voltage was set at 1.5 kV (positive), 3.0kV (negative), sample cone voltage 30V, source temperature at 120° C, cone gas flow 50 L/h and desolvation gas flow rate of 800 L/h with scan time of 0.5 sec in continuum mode. Leucine Enkephalin; 556.2771 Da (positive) and 554.2615 Da (negative) was used for lockspray correction and scans were performed at 0.5 min. The injection volume for each sample was 3µL, unless otherwise specified. The acquisition was carried out with instrument auto gain control to optimize instrument sensitivity over the samples acquisition time. LC-MS and LC-MSe data were processed using Progenesis QI (Nonlinear, Waters) and values were reported as area units.
Ion Mode:POSITIVE
  
MS ID:MS002195
Analysis ID:AN002353
Instrument Name:Waters Xevo G2-XS
Instrument Type:QTOF
MS Type:ESI
MS Comments:Mass spectrometry data was acquired using ‘sensitivity’ mode in positive and negative electrospray ionization mode within 50-1200 Da range. For the electrospray acquisition, the capillary voltage was set at 1.5 kV (positive), 3.0kV (negative), sample cone voltage 30V, source temperature at 120° C, cone gas flow 50 L/h and desolvation gas flow rate of 800 L/h with scan time of 0.5 sec in continuum mode. Leucine Enkephalin; 556.2771 Da (positive) and 554.2615 Da (negative) was used for lockspray correction and scans were performed at 0.5 min. The injection volume for each sample was 3µL, unless otherwise specified. The acquisition was carried out with instrument auto gain control to optimize instrument sensitivity over the samples acquisition time. LC-MS and LC-MSe data were processed using Progenesis QI (Nonlinear, Waters) and values were reported as area units.
Ion Mode:POSITIVE
  
MS ID:MS002196
Analysis ID:AN002354
Instrument Name:Waters Xevo G2-XS
Instrument Type:QTOF
MS Type:ESI
MS Comments:Mass spectrometry data was acquired using ‘sensitivity’ mode in positive and negative electrospray ionization mode within 100-2000 Da for complex lipids. For the electrospray acquisition, the capillary voltage was set at 1.5 kV (positive), 3.0kV (negative), sample cone voltage 30V, source temperature at 120° C, cone gas flow 50 L/h and desolvation gas flow rate of 800 L/h with scan time of 0.5 sec in continuum mode. Leucine Enkephalin; 556.2771 Da (positive) and 554.2615 Da (negative) was used for lockspray correction and scans were performed at 0.5 min. The injection volume for each sample was 3µL, unless otherwise specified. The acquisition was carried out with instrument auto gain control to optimize instrument sensitivity over the samples acquisition time. LC-MS and LC-MSe data were processed using Progenesis QI (Nonlinear, Waters) and values were reported as area units.
Ion Mode:POSITIVE
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