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Anti e cadherin monoclonal antibody

Manufactured by Abcam

Anti-E-cadherin monoclonal antibody is a laboratory reagent used in various research applications. It is a protein that specifically binds to and detects the E-cadherin protein, which is important for cell-cell adhesion. The antibody can be used in techniques such as immunohistochemistry, Western blotting, and flow cytometry to study the expression and localization of E-cadherin in biological samples.

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2 protocols using anti e cadherin monoclonal antibody

1

Cytoskeletal and Focal Adhesion Protein Detection

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The following primary monoclonal and polyclonal antibodies were used to detect cytoskeletal and FA proteins by immunofluorescent labeling and immunoblot analysis: anti-GAPDH monoclonal antibody (Cat. No. ab8245, Abcam, Cambridge, MA), anti-secretoglobin family 1A member 1 (CC10/scgb1a1; Cat. No. 213202, Abcam), anti-E-cadherin monoclonal antibody (Cat. No. 610181, BD Bioscience, San Jose, CA), total paxillin (PAX; Cat. No. 2542, Cell Signaling, Danvers, MA), phospho-PAX Tyr118 (pPAX; Cat. No. 2541, Cell Signaling), total focal adhesion kinase (FAK; Cat. No. 3285, Cell Signaling), phospho-FAK Tyr397 (pFAK, Cat. No. 3283, Cell Signaling), phospho-MLC2 (pMLC2; Cat. No. 3671t, Cell Signaling), MLC2 (Cat. No. 8505s, Cell Signaling), and RhoA (Cat. No. 2117s, Cell Signaling). Alexa Fluor 488 (Cat. No. A12379) and 633 (Cat. No. A22284) phalloidin as well as anti-rabbit and anti-mouse secondary antibodies conjugated to Alexa Fluor 488, 568, or 633 (Cat. Nos. A-21206, A-10042, and A-21050) dyes were obtained from Thermo Fisher Scientific (Waltham, MA). The specificity of antibodies against MLC2 and pMLC2 has been reported previously (49 (link)–51 (link)). ROCK inhibitor Y-27632 was purchased from Millipore Sigma (Cat. No. SCM075, St. Louis, MO) and resuspended in deionized water. Y-27632 inhibits both ROCK1 and ROCK2 by competing with ATP for binding to the catalytic site (52 (link)).
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2

Immunohistochemical Analysis of E-Cadherin

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After dissection, tumors were fixed in 4% paraformaldehyde, followed by dehydration in 30% glucose. Immunohistochemistry was performed on the tumor frozen sections. Rat anti-E-Cadherin monoclonal antibody (Abcam, 1:200) and cy5.5 conjugated second antibody were used to stain the epithelial cell marker. Tumor cells were cultured on glass-bottom chamber slides. After various treatments, the cells were fixed in 4% paraformaldehyde, followed by E-Cadherin staining.
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