Lipidomics studies on macrophages - Foam cell study with wild-type and LDLR(-/-) mice, normal and high-fat diets

Introduction | Browse | Download
Mouse-over the above links for more information
Legend:graph_icon: View data for technical replicates
graph icon: Graph of technical replicates(within an expt.) graph icon: Graph of biological replicates(across expts.)
Details/Graph
technical replicates
LM_ID NameMass
(neutral)		 WT-Fat
WT-Chow
KO-Fat
KO-Chow		 Units
. . . .
(BCJ070124)LMFA03000002 11(12)-EpETE318.2 (ions) -
0.37
0.3
0.37		 pmol/1E6 cells
(BCJ070124)LMFA03060085 11-HETE320.2 (ions) 0.7
0.47
0.37
0.97		 pmol/1E6 cells
(BCJ070124)LMFA03060088 12-HETE320.2 (ions) 120
130
72
160		 pmol/1E6 cells
(BCJ070124)LMFA03060019 12-oxo-ETE318.2 (ions) -
1.5
1.8
2.1		 pmol/1E6 cells
(BCJ070124)LMFA03000003 14(15)-EpETE318.2 (ions) -
3
3.1
1.9		 pmol/1E6 cells
(BCJ070124)LMFA03010051 15-deoxy-PGD2334.2 (ions) 1.6
2.6
3.8
1.9		 pmol/1E6 cells
(BCJ070124)LMFA03010021 15-deoxy-PGJ2316.2 (ions) 0.83
1.6
22
30		 pmol/1E6 cells
(BCJ070124)LMFA03060087 15-HETE320.2 (ions) 26
10
1.5
16		 pmol/1E6 cells
(BCJ070124)LMFA03060009 20-HETE320.2 (ions) 8.4
12
17
13		 pmol/1E6 cells
(BCJ070124)LMFA03030003 2,3-Dinor-TXB2342.2 (ions) 3.3
2.4
3.1
2.8		 pmol/1E6 cells
(BCJ070124)LMFA03060024 5-HETE320.2 (ions) 5.5
3.1
1.8
3.4		 pmol/1E6 cells
(BCJ070124)LMFA03000001 8(9)-EpETE318.2 (ions) -
1.4
-
-		 pmol/1E6 cells
(BCJ070124)LMFA03060086 8-HETE320.2 (ions) 12
5.4
6
15		 pmol/1E6 cells
(BCJ070124)LMFA08040001 AA-EA347.3 (ions) 0.8
0.85
0.87
1		 pmol/1E6 cells
(BCJ070124)LMFA01030001 Arachidonic acid304.2 (ions) 3.5
2.5
3.6
3.2		 pmol/1E6 cells
(BCJ070124)LMFA03020002 LTE4439.2 (ions) 5.9
5.1
7.4
4.3		 pmol/1E6 cells
(BCJ070124)LMFA03010004 PGD2352.2 (ions) 20
7.4
5
16		 pmol/1E6 cells
(BCJ070124)LMFA03010003 PGE2352.2 (ions) 17
9.2
3.7
32		 pmol/1E6 cells
(BCJ070124)LMFA03010019 PGJ2334.2 (ions) 1.1
2.1
2.1
2.3		 pmol/1E6 cells
(BCJ070124)LMFA03030002 TXB2370.2 (ions) 29
33
14
46		 pmol/1E6 cells

 


*:The units in the table and graphs correspond to the intensity of each analyte divided by the intensity of the corresponding deuterated internal standard. The amount of internal standard added to each sample in the time series and control experiments was identical. The relative intensity values were converted to pmoles by extrapolating from the standard curve for that analyte and then normalized to the number of cells in a given sample as measured by the quantity of DNA in the well.