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The band intensity in Western blot analysis was quantified by ImageJ.
Meanwhile, metal analysis was quantified by Inductively Coupled Plasma Mass Spectrometry (ICP/MS) to estimate the amounts of trace metals in DOTA-NHS and ensure radiolabeling efficiency of the conjugate at the radiopharmacy.
The overall performance of the ROC analysis was quantified by computing area under the curve (AUC).
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In present practices, residual stresses needed for strength, deflection and crack width analysis are quantified by means of standard bending tests.
The results of Western Blot analysis were quantified by measuring the relative intensity compared to the control by using Kodak Molecular Imaging Software (Version 4.0.5, Eastman Kodak Company, Rochester, NY, USA) and represented in the relative intensities.
The samples used in the RNA-Seq analysis were quantified by real-time RT-PCR.
Gene expression levels of the samples used for microarray analysis were quantified by quantitative reverse transcriptase PCR (RT-qPCR).
The dot intensities of apoptosis membrane arrays for semi-quantitative analysis were quantified by volume densitometry using BioRad Image Lab software.
For semi-quantitative analysis, protein expression was quantified by densitometric analysis using Quantity One 4.6.5 (Bio-Rad).
For Western-blotting analysis, band intensity was quantified by densitometry using ImageQuant software (v5.2, Molecular Dynamics).
In the data analysis, mRNA expression was quantified by a Nikon Eclipse E800 microscope as a brown reaction.
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