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AB11350

Anti-beta Catenin (phospho S33 + S37) antibody [BC-22]

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(12 Publications)

Mouse Monoclonal beta Catenin phospho S33 + S37 antibody. Suitable for WB and reacts with Human samples. Cited in 12 publications.

View Alternative Names

CTNNB, OK/SW-cl.35, PRO2286, CTNNB1, Catenin beta-1, Beta-catenin

1 Images
Western blot - Anti-beta Catenin (phospho S33 + S37) antibody [BC-22] (AB11350)
  • WB

Supplier Data

Western blot - Anti-beta Catenin (phospho S33 + S37) antibody [BC-22] (AB11350)

Lane 1:

Western blot - Anti-beta Catenin (phospho S33 + S37) antibody [BC-22] (ab11350) at 3.5 µg/mL

Lane 2:

Negative control: without primary antibody

All lanes:

HEK-293 whole cell lysate

Secondary

All lanes:

Goat Anti-Mouse IgG-Peroxidase

Predicted band size: 85 kDa

false

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

BC-22

Isotype

IgG2b

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

Storage in frost-free freezers is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7.4 Preservative: 0.097% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Beta Catenin also known by names such as CTNNB1 or beta-chip is an important protein involved in cell signaling and adhesion. This protein has a molecular weight of around 88 kDa. Beta Catenin is expressed in many cell types and tissues indicating its widespread role in various biological processes. It functions mechanically by mediating the linkage between cadherins and the actin cytoskeleton facilitating cell-cell adhesion. Beta Catenin is also a central part of transcription regulation processes in the nucleus.
Biological function summary

This protein plays roles in both cell adhesion and the regulation of gene expression. Beta Catenin is a critical component of the Wnt signaling pathway where it can form complexes with other proteins to influence gene transcription. In the absence of Wnt signaling beta Catenin levels are low due to its degradation. However when the pathway is active it accumulates in the cytoplasm and eventually translocates to the nucleus where it interacts with TCF/LEF transcription factors to regulate the expression of target genes.

Pathways

Beta Catenin plays a central role in the Wnt signaling pathway and influences cell fate decisions and cellular proliferation. It acts in concert with proteins such as Dishevelled (DVL) and Axin to coordinate these important biological processes. In the absence of Wnt signaling proteins such as APC and GSK-3β are responsible for beta Catenin degradation keeping its cellular levels in check. Beta Catenin’s interaction with transcription factors in the nucleus makes it pivotal in the regulation of cell and tissue homeostasis.

Beta Catenin has associations with colorectal cancer and hepatocellular carcinoma. Its dysregulation can lead to unchecked cell proliferation and tumorigenesis. Often mutations in the beta Catenin gene (CTNNB1) or components of the Wnt pathway like APC are implicated in the development of these cancers. Its interplay with E-cadherin is important for maintaining tissue architecture and disruptions can lead to invasive cancer phenotypes. Understanding beta Catenin’s role provides insights into therapeutic strategies for these cancers.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Key downstream component of the canonical Wnt signaling pathway (PubMed : 17524503, PubMed : 18077326, PubMed : 18086858, PubMed : 18957423, PubMed : 21262353, PubMed : 22155184, PubMed : 22647378, PubMed : 22699938). In the absence of Wnt, forms a complex with AXIN1, AXIN2, APC, CSNK1A1 and GSK3B that promotes phosphorylation on N-terminal Ser and Thr residues and ubiquitination of CTNNB1 via BTRC and its subsequent degradation by the proteasome (PubMed : 17524503, PubMed : 18077326, PubMed : 18086858, PubMed : 18957423, PubMed : 21262353, PubMed : 22155184, PubMed : 22647378, PubMed : 22699938). In the presence of Wnt ligand, CTNNB1 is not ubiquitinated and accumulates in the nucleus, where it acts as a coactivator for transcription factors of the TCF/LEF family, leading to activate Wnt responsive genes (PubMed : 17524503, PubMed : 18077326, PubMed : 18086858, PubMed : 18957423, PubMed : 21262353, PubMed : 22155184, PubMed : 22647378, PubMed : 22699938). Also acts as a coactivator for other transcription factors, such as NR5A2 (PubMed : 22187462). Promotes epithelial to mesenchymal transition/mesenchymal to epithelial transition (EMT/MET) via driving transcription of CTNNB1/TCF-target genes (PubMed : 29910125). Involved in the regulation of cell adhesion, as component of an E-cadherin : catenin adhesion complex (By similarity). Acts as a negative regulator of centrosome cohesion (PubMed : 18086858). Involved in the CDK2/PTPN6/CTNNB1/CEACAM1 pathway of insulin internalization (PubMed : 21262353). Blocks anoikis of malignant kidney and intestinal epithelial cells and promotes their anchorage-independent growth by down-regulating DAPK2 (PubMed : 18957423). Disrupts PML function and PML-NB formation by inhibiting RANBP2-mediated sumoylation of PML (PubMed : 22155184). Promotes neurogenesis by maintaining sympathetic neuroblasts within the cell cycle (By similarity). Involved in chondrocyte differentiation via interaction with SOX9 : SOX9-binding competes with the binding sites of TCF/LEF within CTNNB1, thereby inhibiting the Wnt signaling (By similarity). Acts as a positive regulator of odontoblast differentiation during mesenchymal tooth germ formation, via promoting the transcription of differentiation factors such as LEF1, BMP2 and BMP4 (By similarity). Activity is repressed in a MSX1-mediated manner at the bell stage of mesenchymal tooth germ formation which prevents premature differentiation of odontoblasts (By similarity).
See full target information CTNNB1 phospho S33 + S37

Publications (12)

Recent publications for all applications. Explore the full list and refine your search

Aging 13:25903-25919 PubMed34910686

2021

METTL14 benefits the mesenchymal stem cells in patients with steroid-associated osteonecrosis of the femoral head by regulating the m6A level of PTPN6.

Applications

Unspecified application

Species

Unspecified reactive species

Cheng Cheng,Haoping Zhang,Jia Zheng,Yi Jin,Donghui Wang,Zhipeng Dai

European journal of histochemistry : EJH 64: PubMed33131270

2020

Swertiamarin suppresses proliferation, migration, and invasion of hepatocellular carcinoma cells <em>via</em> negative regulation of FRAT1.

Applications

Unspecified application

Species

Unspecified reactive species

Shufeng Xiao,Haoren Tang,Yao Bai,Renchao Zou,Zongfang Ren,Xuesong Wu,Zhitian Shi,Song Lan,Wei Liu,Tiangen Wu,Cheng Zhang,Lin Wang

Frontiers in cell and developmental biology 8:862 PubMed33015048

2020

The Role of Wnt/β-Catenin Pathway Mediators in Aortic Valve Stenosis.

Applications

Unspecified application

Species

Unspecified reactive species

Kashif Khan,Bin Yu,Chrystina Kiwan,Yousif Shalal,Sabin Filimon,Megan Cipro,Dominique Shum-Tim,Renzo Cecere,Adel Schwertani

Journal of cellular and molecular medicine 24:9658-9666 PubMed32667746

2020

Oestrogen induces epithelial-mesenchymal transition in endometriosis via circ_0004712/miR-148a-3p sponge function.

Applications

Unspecified application

Species

Unspecified reactive species

Xin He,Nana Liu,Tianyi Mu,Dan Lu,Chanwei Jia,Shuyu Wang,Chenghong Yin,Lingyan Liu,Liying Zhou,Xiaowu Huang,Yanmin Ma

RSC advances 10:7221-7231 PubMed35493872

2020

Retracted Article: CircBANP acts as a sponge of let-7a to promote gastric cancer progression the FZD5/Wnt/β-catenin pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Jin Xun,Chunfeng Wang,Jianning Yao,Bing Gao,Lianfeng Zhang

Journal of Cancer 11:2201-2212 PubMed32127947

2020

Lnc-SNHG16/miR-128 axis modulates malignant phenotype through WNT/β-catenin pathway in cervical cancer cells.

Applications

Unspecified application

Species

Unspecified reactive species

Wu Wu,Li Guo,Zhenlong Liang,Yuanbin Liu,Zhi Yao

PloS one 14:e0218135 PubMed31242206

2019

Expression of serine/threonine protein kinase SGK1F promotes an hepatoblast state in stem cells directed to differentiate into hepatocytes.

Applications

Unspecified application

Species

Unspecified reactive species

Fouzeyyah Alsaeedi,Rachel Wilson,Charlotte Candlish,Ibrahim Ibrahim,Alistair C Leitch,Tarek M Abdelghany,Colin Wilson,Lyle Armstrong,Matthew C Wright

Bioscience reports 39: PubMed31196962

2019

Inhibition of GLS suppresses proliferation and promotes apoptosis in prostate cancer.

Applications

Unspecified application

Species

Unspecified reactive species

Junfeng Zhang,Shiyu Mao,Yadong Guo,Yuan Wu,Xudong Yao,Yong Huang

Journal of cellular biochemistry 120:15429-15442 PubMed31111563

2019

microRNA-96 promotes osteoblast differentiation and bone formation in ankylosing spondylitis mice through activating the Wnt signaling pathway by binding to SOST.

Applications

Unspecified application

Species

Unspecified reactive species

Shu Ma,Dan-Dan Wang,Cheng-Yuan Ma,Yan-Dong Zhang

Cells 8: PubMed31013745

2019

YAP, ΔNp63, and β-Catenin Signaling Pathways Are Involved in the Modulation of Corneal Epithelial Stem Cell Phenotype Induced by Substrate Stiffness.

Applications

Unspecified application

Species

Unspecified reactive species

Ricardo M Gouveia,Flora Vajda,Jason A Wibowo,Francisco Figueiredo,Che J Connon
View all publications

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