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The membrane was then submerged in ECL developing solution (GE Healthcare, RPN2232) and the data were quantified using the array analyzer software (Active Motif).
The data were quantified using a FUJI FLA-5000 imager.
The data were quantified using a Bioscan IAR-2000 TLC scanner (Washington, DC, USA).
The hybridized images were analyzed using an Agilent DNA Microarray Scanner (Agilent Technology, USA), and the data were quantified using the Agilent Feature Extraction software (Agilent Technology, USA).
The data were quantified using the LICOR Odyssey system relative to non specific bands (** and *, Figure 5 figure supplement 2B ) to control for loading.
The hybridization images were analyzed using an Agilent DNA Microarray Scanner (Agilent Technology, USA), and the data were quantified using the Agilent Feature Extraction software (Agilent Technology, USA).
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Tests were also run in a Bayesian framework, where the relative support of competing hypotheses given the data was quantified using the Bayes factor (BF) [ 66].
The PCR data were quantified using the 2−∆∆Ct method, by comparing signal of the sh-RNA treated groups with that of the control group, both relative to an internal control, β-actin.
The obtained data were quantified using the relative standard method.
The emission data were quantified using the cycle threshold value.
Signal from the membranes was collected from an Epi Chemi II darkroom unit fitted with a CCD camera (UVP, San Gabriel, CA, USA) and the resulting data were quantified using LabWorks Image Acquisition software (UVP) and/or Image J software (http://rsb.info.nih.gov/ij/).
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