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Images were generated with the GenePix software and data from duplicate spotted protein binding were normalized with respect to anti-actin binding.
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All binding curves were normalized with a blank flow cell and a control curve of the empty analyte injection.
The mRNA values were normalized with TATA binding protein (TBP) serving as the internal control.
The input files were normalized with full quantile normalization [95].
To compare the results obtained with different vesicle preparations, binding was normalized against the value determined in the absence of recombinant proteins.
For each brain, specific binding was normalized to the average specific binding from brains in the vehicle-treated group.
Samples were normalized with creatinine.
H3K9ac levels were normalized with H3 levels.
Urinary concentrations were normalized with specific gravity (SG).
N-glycosylation data were normalized with sum of values.
All blots were normalized with β-tubulin.
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