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Antibody against β catenin

Manufactured by BD
Sourced in Switzerland, United States

The Antibody against β‐catenin is a laboratory reagent used for the detection and analysis of β‐catenin, a key protein involved in cellular signaling pathways. This antibody can be utilized in various immunoassay techniques, such as Western blotting, immunohistochemistry, and immunocytochemistry, to investigate the expression and localization of β‐catenin in biological samples.

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3 protocols using antibody against β catenin

1

Western Blot Antibody Profiling

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Antibodies against Flag-M2, hnRNPK/J and β-actin were purchased from Sigma-Aldrich. Antibody against GAPDH was obtained from ENOGENE. Antibody against β-catenin was acquired from BD Biosciences. Antibody against Twist was purchased from GeneTex. Antibody against Aurora-A was obtained from Abcam as was anti-mono/dimethyl arginine antibody. Finally, a specific antibody was custom ordered from GeneTex that allowed detection of hnRNPK S379 phosphorylation.
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2

Immunohistochemical Analysis of Liver β-Catenin

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Immunohistochemical analysis was performed on liver biopsy sections using an avidin‐biotin complex method (ABC detection kit, Vector Laboratories, Petersborough, UK). Following pressure cooker‐mediated antigen retrieval in 0.001 M ethylenediaminetetraacetic acid, pH 8, the sections were incubated with 10% goat serum (Dako Cytomation, Baar, Switzerland) for 20min. Endogenous peroxidase activity was blocked using 0.5% H2O2. Slides were then incubated with an antibody against β‐catenin (BD Biosciences, Allschwil, Switzerland) at a dilution 1:200. The labeling index was calculated in ‘hot‐spot’ areas as the proportion of positive nuclei as a percentage of the total number of nuclei.
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3

Western Blot Protocol for Cell Lysates

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For isolation of total lysates, cells were pelleted after 1× PBS wash and lysed in RIPA lysis buffer (Thermo #89900) supplied with protease inhibitor cocktail (Sigma #11836170001). Lysates were collected in new pre‐chilled tubes and protein concentration was measured using Bradford reagent (Bio‐Rad #500‐025) and BSA standards (Bio‐Rad #500‐027). Equal amount of protein was mixed with 4× gel loading dye (Thermo #NP007) and analyzed by pre‐casted gel (Thermo #NP0036) and Western blotting. Final western blots were detected on a GE Healthcare Life Sciences, Amersham Imager 600, followed by analyzing band intensities with ImageJ (U.S. National Institutes of Health, Bethesda, MD, USA).
Antibodies used for western blotting were as follows: anti‐LRP6 (#S2560) primary antibody was purchased from Cell Signaling Technology, antibody against anti‐GAPDH (#GTX627408) was from GeneTex, anti‐Vinculin (#sc‐736914) primary antibody was from Santa Cruz, antibody against β‐catenin (#610153) was from BD Biosciences, anti‐MCL‐1 (#ab32087), anti‐BCL‐2 (#ab692) primary antibodies were from Abcam.
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