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Bands were quantitated using the integrated density function of ImageJ.
Bands were quantitated using National Institute of Health's ImageJ software.
Gels were vacuum dried, and Dvl1-3 protein bands were quantitated using a Typhoon phosphorimager with ImageQuant software (Molecular Dynamics).
Bands were quantitated using reverse image scanning densitometry (Photoshop CS2, Adobe) by normalizing the band intensity of the co-immunoprecipitated protein to the band intensity of the immunoprecipitated protein.
Radiolabeled bands were quantitated using a phosphorimager.
The bands were quantitated using ImageQuant software.
Similar(43)
The optical density of bands was quantitated using the ImageJ v.1.38 software and the ratios to GAPDH were normalized for time 0 hr and then expressed as fold- values of the mean±SEM.
The density of the respective bands was quantitated using a densitometer with AlphaView Software for FluorChem Systems (ProteinSimple™).
The intensity of bands was quantitated using 'Phoretix 1D Advanced' software as above.
The intensity of protein bands was quantitated using Lab Works 4.0 software (UVP Inc., Upland, CA, USA).
The integrated optical density of bands was quantitated using the Image J v.1.47 software.
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