spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.



Fig. 8. Activation of the ERK pathway by ß-catenin overexpression, and effects of dominant-negative Tcf-4 on ß-catenin-induced ERK pathway activation. (A) NIH3T3 cells were grown in DMEM and transfected with either 0.5 µg pcDNA3.0 vector or 0.5 µg Flag-ß-catenin-pcDNA3.0. Cells were harvested 48 hours after transfection. (B) NIH3T3 cells were grown in DMEM and transfected with either 0.5 µg pcDNA3.0 vector or 0.5 µg Flag-ß-catenin-pcDNA3.0. Where required, cells were treated with 20 µM U0126 1 hour before harvesting. Anti-Flag antibody was used for detection of Flag-ß-catenin. (C) NIH3T3 cells were grown in DMEM and transfected with either 0.5 µg pcDNA3.0 vector or 0.5 µg Flag-ß-catenin-pcDNA3.0. Cells were co-transfected with 0.5 µg of vector or {Delta}N-Tcf-4E together with Flag-ß-catenin-pcDNA3.0. The cells were harvested after 48 hours and western blot analyses were performed with ß-catenin, Flag, ERK, p-ERK, p-MEK, Raf-1 or {alpha}-tubulin antibodies.





Right arrow Return to article