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 data were quantified using the LICOR Odyssey system relative to non specific bands (** and *, Figure 5 figure supplement 2B ) to control for loading.
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 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).
The data were quantified using the MetaXpress software and integrated fluorescence intensity (average fluorescence intensity per pixel) of the whole image was plotted against the CGP 20712A concentrations used.
The quantitative-PCR data was quantified using the comparative quantitation analysis program of MxPro Q-PCRanalysis software version 3.0 (Stratagene).
The impact of US imaging on MR data was quantified using the signal-to-noise ratio (SNR) calculated in a circular region of interest (ROI) located wholly within the cryogel.
The RT-qPCR expression level data was quantified using the Comparative CTT (ΔΔCT) method and relative abundance of the sgRNA was normalized to the mRNA transcript UBC6, which was used as the endogenous control (Teste et al., 2009).
The raw TIFF-image data was quantified using Imagene (v5).
