d dynasore. All values are relative expression levels compared to controls from cells incubated with control-conditioned medium and transfected with an empty plasmid. Results are presented as the mean fold change 
SEM from 3 independent experiments. Immunoblotting Samples of 1050 g total protein were subjected to SDS-PAGE. Resolved proteins were transferred to nitrocellulose membrane, which was blocked in 5% skim milk, probed with specific antibodies and detected by enhanced chemiluminescence on ImageQuant LAS 4000 or Odyssey PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/1974422 infrared imaging system. Antibodies The following primary antibodies were used: anti-Tollip, anti-ubiquitin, anti-ubiquitin Lys48-specific, anti-ubiquitin Lys63-specific, anti-myc, anti-HA, anti–catenin, anti-active -catenin, anti-dynamin, anti–tubulin, anti–actin, anti-GAPDH and anti-vinculin. All primary antibodies were used at dilution of 1:1000 for immunoblotting. Secondary peroxidase-conjugated antibodies were purchased from Jackson ImmunoResearch and fluorophore-conjugated from LI-COR Biosciences. All secondary antibodies for immunoblotting were used at dilution of 1:10000. For immunofluorescence, Alexa-conjugated secondary antibodies were used at dilution of 1:500. Immunoprecipitation Cells were seeded on 100 mm culture plates and the next day transfected with plasmids encoding Tollip and HA-tagged ubiquitin. For immunoprecipitation of -catenin cells were grown for 24 h and treated for the last 4 h before lysis with 5 M MG132. For immunoprecipitation of Tollip, transfected cells were grown for 48 h and incubated for the last 18 h prior to lysis with Wnt3a-conditioned medium in the presence or absence of 5 M MG132. After 24 or 48 h cells were washed once with PBS and lysed using RIPA buffer containing 5 mM N-ethylmaleimide at 4C. Lysates were clarified from cell debris by centrifugation and DNA was sheared using Qiashredder columns. After preclearance for 3 h PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19740492 with nonspecific immunoglobulins, bound proteins were depleted using Protein A or G agarose for 1 h. Precleared cell lysates were then incubated overnight at 4C with the indicated antibodies coupled to Protein A or G 6 / 27 Tollip Inhibits Canonical Wnt Signaling agarose. The agarose beads were washed four times using IP buffer before elution with 0.1 M glycine of pH 2.5. Finally samples were analyzed by SDS-PAGE and immunoblotting. Immunofluorescence and microscopy HEK293 cells were seeded on 12-mm gelatin-coated coverslips in a 24-well plate. The coverslips were incubated in 0.2% gelatin for 30 min at 4C prior to plating. The next day cells were transfected with DNA using Lipofectamine2000 or with siRNA using HiPerFect according to the manufacturer’s instructions. After 24 h or after 72 h cells were stimulated with Wnt3a-conditioned medium or controlconditioned medium for the indicated time, rinsed with PBS containing 1 mM CaCl2 and 0.5 mM MgCl2 and fixed with 3.6% paraformaldehyde in PBS for 15 min at room temperature. Next, cells were permeabilized with 0.1% Triton X-100 and blocked using 10% fetal bovine serum in PBS for 30 min. Cells were further incubated overnight with primary antibodies against: -catenin, Tollip or myc tag. Next day, cells were incubated with get R115777 appropriate Alexa-conjugated secondary antibodies and DAPI in 5% fetal bovine serum in PBS. For quantitative analysis at least ten randomly selected regions were imaged for each experimental condition. Single confocal plane images were acquired with Zeiss LSM710 microscope using 40x/1.30
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