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Western blot images from (A) experiments were quantified with densitometry using Quantity One Basic software (BioRad).
The target bands on the Western Blots from three experiments were quantified with a NIH Image software.
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The fluorescence signals of tRNA-ProUGG images of three independent experiments were quantified, and the average NAIs with SDVs were calculated.
The results from three separate experiments were quantified and plotted.
The changes in selectivity and flux were quantified with permeation experiments.
After the experiment, femoral cortical and trabecular bone structure were quantified with μCT in the mid-diaphysis and distal epiphysis, respectively, and entheseal morphology was quantified in the lateral epicondyle.
After the experiment, femoral cortical and trabecular bone structure were quantified with micro-CT in the mid-diaphysis and distal metaphysis, respectively, and diaphyseal structural strength was determined with mechanical testing.
The BRET experiments were performed with cells in suspension and were quantified with a Pherastar (BMG) (22).
The optimized bio-stimulation conditions were quantified with response surface methodology (RS M experiments based on a Box Behnken design (Chen et al. 2007).
Images were quantified with Imagene v.7.
Bands were quantified with Chemi Doc software.
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