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2 protocols using galectin 1

1

Affinity Purification and Immunoblotting Protocol

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Affinity purification using anti-FLAG agarose (Millipore Sigma, St. Louis, MO, USA), glutathione-agarose (Millipore Sigma), and TALON resin (Clontech, Mountain View, CA, USA) was done as described [16 (link)–19 (link)]. Immunoblot analysis was performed using antibodies purchased from Santa Cruz Biotechnology [(Myc tag (9E10), sc-40; actin, sc-1616-R; dynein heavy chain, sc-9115; ß-catenin, sc-7199; γ-catenin, sc-7900; Src, sc-18; desmoplakin, sc-33555; c-Myc, sc-764; Enigma, sc-98370; Galectin 1, sc-28248; EGFR, sc-03; phosphotyrosine (PY99), sc-7020], Cell Signaling Technology (Beverly, MA, USA) [EGFR, #4267; c-Met, #3127; HER2, #2165; PKCδ, #2058; phospho-PKCδ[Y311], # 2055; CDCP1, #4115 and #13794; P-CDCP1[Y707], #13111; P-CDCP1[Y734], #9050; P-CDCP1[Y743], #13093; P-CDCP1[Y806], #13024; β1-integrin, #4706; MMP14, #13130; P-EGFR[Y845], #6963; P-EGFR[Y992], #2235; P-Src[Y416], #6943; p62, #5114; α-E-catenin, #3236], BD Transduction Laboratories (San Jose, CA, USA) [E-cadherin, 610182; plasminogen activator inhibtor-1 (PAI-1), 612024], BD Biosciences (San Jose, CA, USA) [p120 catenin, 610133], Neomarkers (Freemont, CA, USA) [cyclin D1, MS-210], EMD Millipore (Temecula, CA, USA) [anti-phosphotyrosine (4G10), 05-321], Invitrogen [desmoglein 2, 32-6100], Qiagen (Valencia, CA, USA) [anti-His5, 34660], and Millipore Sigma [anti-FLAG (M2), F3165].
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2

Immunoprecipitation and Antibody Array Analysis

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For immunoprecipitation, 50 uL of protein G magnetic beads (PureProteome, Millipore) were crosslinked with 10 ug anti-RECK goat polyclonal antibody (R&D) or goat polyclonal IgG antibody (R&D) using 5 mM BS3 according to manufacturer instructions (protocol guide, Millipore). Confluent Hs606.T whole cell lysates (500 ug total protein) were incubated with crosslinked beads at 4°C overnight with gentle agitation. The immunocomplexes were washed 3 times with TBS-T (0.1%), bound protein eluted in 60 uL 0.2 M glycine-HCl (pH 2.5), and neutralized using 5 uL of 1 M Tris (pH 8.5). Eluates were then used to probe an antibody array (Human Soluble Receptor Antibody Array, Non-Hematopoietic Panel, R&D). This array was modified by using IP eluate instead of conditioned media or cell lysate. Eluates were also subjected to SDS-PAGE and Western blotting analysis for RECK (goat antibody, R&D), uPAR (goat antibody, R&D), Galectin-1 (rabbit antibody, Cell Signaling), and Integrin β1 (rabbit antibody, Cell Signaling).
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