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Response magnitudes for each unit were normalized to the maximum response for all stimuli.
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These signal intensities, shown in arbitrary units, were normalized to the highest value set as 100%.
For each experiment, the fluorescence of the transgenic sample, expressed in arbitrary units, was normalized to the two WT samples averaged together.
Values shown (Y axis represents relative expression units) are normalized to GAPDH.
Expression values for each probe set were normalized to zero mean and unit variance.
All relative light unit values were normalized to total protein as described [ 39].
Arbitrary luciferase activity (relative light units) values were normalized to β-galactosidase activity to account for variations in transfection efficiency.
The relative fluorescence units (RFU) were normalized to total protein content, which was determined as for the caspase assays described earlier.
Phenotypes within each population were normalized to zero mean and unit variance prior to the analysis.
The resulting complex values were normalized to unit amplitude.
Cu,Zn-SOD and GPx-1 values were normalized to units per gram of hemoglobin.
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