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Time constants or 1/Rate measures were normalized for the measure of the first burst in the 5 burst sequence.
All measures were normalized for the area of the membrane used in the experimental procedure and expressed as ohm/cm.
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Also, in order to take into account the fact that publication and citation practices vary according to fields, these scientific impact measures were normalized by the world average for each subfield [37] [38].
Access scores for the First Contact Access and First Contact Utilization measures were normalized.
All measured forces were normalized for CSA.
Mander's fractions were measured using thresholding, and values were normalized for each of at least three independent experiments, and statistical significance was determined using two-tailed Student's t-test.
Fluorescence intensities were measured using a spectrofluorimeter and fluorescence values were normalized for DNA content after subtraction of autofluorescence from experimental values, as previously described [ 32].
The amount of f-V122I TTR associated with the cells was measured by fluorescence intensity and the data were normalized for total protein content in the samples.
Data were normalized for transfection efficiency by measuring the mRNA levels of Luc for each experimental point, measured by real-time PCR using SYBRGreen PCR kit (ABI).
For this assay, the units were normalized for total protein content measured with the Bio-Rad protein assay reagent.
Data were normalized for the Renilla activity measured in the same sample.
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