
Phospho-Catenin-beta (Ser37) Rabbit Polyclonal Antibody#abs130893
Please note that the price mentioned is only for your reference. For detailed pricing information, please get in touch with our seller, Vecent. We recommend reaching out to Vecent for accurate and up-to-date pricing details. Data Examples Western blot analysis of Catenin-β phosphorylation...
Description
Catalog-specification | Delivery time | USD price |
abs130893-50ug | 1-2 Weeks | 201 |
abs130893-100ug | 1-2 Weeks | 301 |
Please note that the price mentioned is only for your reference. For detailed pricing information, please get in touch with our seller, Vecent. We recommend reaching out to Vecent for accurate and up-to-date pricing details.
Overview | |
Description | The protein beta-catenin is a crucial component of adherens junctions, which are responsible for creating and maintaining epithelial layers in various organs. These junctions serve multiple functions, including mediating cell adhesion, signaling the presence of neighboring cells, and anchoring the actin cytoskeleton. Through these roles, adherens junctions play a vital role in regulating normal cellular growth and behavior. |
Other names | Beta catenin, also known as catenin (cadherin associated protein), beta 1, 88kDa, is a cadherin associated protein that plays an important role in cell adhesion and cell signaling pathways. It is encoded by the CTNNB1 gene and is involved in the Wnt signaling pathway, which is important for embryonic development and tissue homeostasis. Beta-catenin is a key player in regulating cell proliferation, differentiation, and polarity, as well as in tissue regeneration and repair. It is also involved in the development and maintenance of various organs, including the brain, liver, and heart. Additionally, beta-catenin has been implicated in several diseases, such as cancer, Alzheimer's disease, and osteoporosis. Understanding the functions and mechanisms of beta-catenin is critical for the development of effective therapies to treat these diseases. |
Source | Rabbit |
Specificity | This antibody known as Phospho-Catenin-β (Ser37) Antibody is capable of detecting natural levels of Catenin-β when it has been phosphorylated at the Serine 37 site. It is important to note that this antibody will not detect non-phosphorylated Catenin-β. |
| Reactivity | Human;Mouse;Rat |
Predictive reaction species | Zebrafish;Chicken;Rabbit;Xenopus;Dog;Horse;Bovine;Sheep;Pig |
| Antigen | Catenin-β |
Application | IHC 1:50-1:200, WB 1:500-1:2000, IF/ICC 1:100-1:500, and ELISA (peptide) 1:20000-1:40000 are the recommended dilution ranges for different techniques. |
| Immunogen | Catenin-β37。,。 |
Properties | |
| MW | 92kDa |
| Concentration | 1mg/ml |
Purification | ,。,。 |
Clonality | Polyclonal Antibody |
| Stability & Storage | To ensure the longevity of the product, it is recommended to store it at a temperature of -20 °C for a duration of one year. It is important to avoid subjecting the product to repeated freezing and thawing cycles to maintain its quality and effectiveness. |
Storage buffer | The storage conditions for Rabbit IgG are as follows: it should be stored at -20 °C in a solution containing phosphate buffered saline at pH 7.4, 150mM NaCl, 0.02% sodium azide, and 50% glycerol. The stability of the IgG is guaranteed for 12 months from the date of receipt. |
Target | |
Background | Key downstream component of the canonical Wnt signaling pathway. 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. 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. Involved in the regulation of cell adhesion, as component of an E-cadherin:catenin adhesion complex. Acts as a negative regulator of centrosome cohesion. Involved in the CDK2/PTPN6/CTNNB1/CEACAM1 pathway of insulin internalization. Blocks anoikis of malignant kidney and intestinal epithelial cells and promotes their anchorage-independent growth by down-regulating DAPK2. Disrupts PML function and PML-NB formation by inhibiting RANBP2-mediated sumoylation of PML (PubMed:17524503, PubMed:18077326, PubMed:18086858, PubMed:18957423, PubMed:21262353, PubMed:22647378, PubMed:22699938, PubMed:22155184). Promotes neurogenesis by maintaining sympathetic neuroblasts within the cell cycle (By similarity). |
Tissue specificity | Expressed in several hair follicle cell types: basal and peripheral matrix cells, and cells of the outer and inner root sheaths. Expressed in colon. Present in cortical neurons (at protein level). |
| Posttranslational modification | Phosphorylation at Ser-552 by AMPK promotes stabilizion of the protein, enhancing TCF/LEF-mediated transcription (By similarity). Phosphorylation by GSK3B requires prior phosphorylation of Ser-45 by another kinase. Phosphorylation proceeds then from Thr-41 to Ser-37 and Ser-33. Phosphorylated by NEK2. EGF stimulates tyrosine phosphorylation. Phosphorylation on Tyr-654 decreases CDH1 binding and enhances TBP binding. Phosphorylated on Ser-33 and Ser-37 by HIPK2 and GSK3B, this phosphorylation triggers proteasomal degradation (PubMed:25169422). Phosphorylation on Ser-191 and Ser-246 by CDK5. Phosphorylation by CDK2 regulates insulin internalization. Phosphorylation by PTK6 at Tyr-64, Tyr-142, Tyr-331 and/or Tyr-333 with the predominant site at Tyr-64 is not essential for inhibition of transcriptional activity.Ubiquitinated by the SCF(BTRC) E3 ligase complex when phosphorylated by GSK3B, leading to its degradation. Ubiquitinated by a E3 ubiquitin ligase complex containing UBE2D1, SIAH1, CACYBP/SIP, SKP1, APC and TBL1X, leading to its subsequent proteasomal degradation (By similarity).S-nitrosylation at Cys-619 within adherens junctions promotes VEGF-induced, NO-dependent endothelial cell permeability by disrupting interaction with E-cadherin, thus mediating disassembly adherens junctions.O-glycosylation at Ser-23 decreases nuclear localization and transcriptional activity, and increases localization to the plasma membrane and interaction with E-cadherin CDH1.Deacetylated at Lys-49 by SIRT1. |
Celluar localization | Cytoskeleton;Cytosol;Extracellular region or secreted;Nucleus;Plasma Membrane; |
| UniPort | P35222 |
Data Examples

Western blot analysis of Catenin-β phosphorylation expression in 293 whole cell lysates,The lane on the left is treated with the antigen-specific peptide.
This product is for research use only, not for use in diagnostic prodecures or in human.
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