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Exact(15)
All measurements were normalized by actin intensities and then calculated as levels relative to control conditions.
All measurements were normalized by the signal intensity of the surrounding muscle to adjust for image variability.
All measurements were normalized to values from unstretched, untransfected cells.
All measurements were normalized against total protein content from cell lysates.
All measurements were normalized to FM conditions and then corrected for unspecific changes by normalization to respective Ctr constructs, measured under identical conditions.
All measurements were normalized to the base line in this manner using the ratio f-fo/fo.
Similar(45)
All the OD measurements were normalized against the negative control for each microtiter plate separately.
All urine measurements were normalized by urinary creatinine concentration.
All GSH measurements were normalized with total protein levels.
To account for the different proliferation rates under each culture condition, cytokine measurements were normalized to total protein, as quantified via Pierce BCA and phospho-protein measurements were normalized by loading an equal amount of total protein into each assay well and normalized cell lysate loaded into the multiplexed assay to total protein.
Fluorescence measurements were normalized over all 18 microarray chips.
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