Lipidomics studies on macrophages - RAW 264.7 cells treated with Kdo2-Lipid A

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Display Time Course Plots for Selected Analytes
Legendgraph icon: Graph of technical replicates(within an expt.)
graph icon: Graph of biological replicates(across expts.)		  (BXY123456): Experiment Sample Barcode
PA| PC| PE| PG| PI| PS|
Details/Graph
technical/biological
replicates
 Name KLA
Ctl
 0min		 KLA
Ctl
 30min		 KLA
Ctl
 1hr		 KLA
Ctl
 2hrs		 KLA
Ctl
 4hrs		 KLA
Ctl
 8hrs		 KLA
Ctl
 12hrs		 KLA
Ctl
 24hrs		 Units*
. . . .
mag icon graph icon graph icon(MSH060201)PA(36:4)0.00
0.00		 0.10
0.20		 0.80
0.35		 0.60
0.40		 0.35
0.30		 0.65
0.25		 0.60
0.60		 0.50
0.25		 pmol/ug DNA
mag icon graph icon graph icon(MSH060208)PA(36:4)0.55
0.60		 0.65
0.60		 0.75
0.55		 0.85
0.45		 0.85
0.55		 0.40
0.25		 0.90
1.50		 0.45
0.00		 pmol/ug DNA
mag icon graph icon graph icon(MSH060215)PA(36:4)0.30
0.45		 0.55
0.30		 0.50
0.20		 0.40
0.30		 0.35
0.30		 0.30
0.25		 0.50
0.15		 0.20
0.10		 pmol/ug DNA
*:The units in the table and graphs correspond to the intensity of each species divided by the average intensity (peak area) of a set of odd-chain internal standards corresponding to that particular headgroup. No internal standards were available for the PI series so intensity of each species was divided by the the total PI intensity in this case. The amount of internal standard added to each sample in the time series and control experiments was identical. The relative intensity values were then normalized to the measured quantity of DNA present in each RAW cell preparation following treatment with and without Kdo2-lipid A for each time point.