• Human Catenin beta-1 protein (Recombinant) (C-His) (STJP001253)
  • Human Catenin beta-1 protein (Recombinant) (C-His) (STJP001253)
  • Human Catenin beta-1 protein (Recombinant) (C-His) (STJP001253)
  • Human Catenin beta-1 protein (Recombinant) (C-His) (STJP001253)

Human Catenin beta-1 protein (Recombinant) (C-His) (STJP001253)

SKU:
STJP001253

Current Stock:
Host: E. coli
Reactivity: Human
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Recombinant-Human Catenin beta-1-C-His protein was developed from e. coli and has a target region of C-His. For use in research applications.
Formulation: Lyophilized from a 0.22 Mu m filtered solution of 50mM TRIS, 150mM NaCl, pH 8.0. Contact us for customized product form or formulation.
Immunoreactivity: Measured by its binding ability in a functional ELISA. Immobilized Human CD31 at 1 Mu g/mL (100 Mu L/well) can bind Human CTNNB1 with a linear range of 0.3-4.9 Mu g/ml.
Gene Symbol: CTNNB1
Gene ID: 1499
Uniprot ID: CTNB1_HUMAN
Immunogen Region: Met1-Leu781
Immunogen: Active Recombinant Human Catenin beta-1 Protein is produced by E. coli expression system. The target protein is expressed with sequence (Met1-Leu781) of human Beta-catenin (Accession #XP_016861227.1) fused with a 6×His tag at the C-terminus.
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). Expressed in breast cancer tissues (at protein level).
Post Translational Modifications Phosphorylation at Ser-552 by AMPK promotes stabilization of the protein, enhancing TCF/LEF-mediated transcription. 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. Phosphorylated on Ser-33 and Ser-37 by HIPK2 and GSK3B, this phosphorylation triggers proteasomal degradation. 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. Phosphorylation by SRC at Tyr-333 promotes interaction with isoform M2 of PKM (PKM2).promoting transcription activation. 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. Ubiquitinated and degraded following interaction with SOX9. 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. Phosphorylated at Thr-556 by herpes virus 1/HHV-1 leading to CTNNB1 inhibition.
Function 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. Promotes neurogenesis by maintaining sympathetic neuroblasts within the cell cycle. 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. 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. Activity is repressed in a MSX1-mediated manner at the bell stage of mesenchymal tooth germ formation which prevents premature differentiation of odontoblasts.
Protein Name Catenin Beta-1
Beta-Catenin
Database Links Reactome: R-HSA-195253
Reactome: R-HSA-196299
Reactome: R-HSA-201681
Reactome: R-HSA-201722
Reactome: R-HSA-3134973
Reactome: R-HSA-351906
Reactome: R-HSA-3769402
Reactome: R-HSA-381771
Reactome: R-HSA-4086398
Reactome: R-HSA-418990
Reactome: R-HSA-4411364
Reactome: R-HSA-4641262
Reactome: R-HSA-5218920
Reactome: R-HSA-525793
Reactome: R-HSA-5339716
Reactome: R-HSA-5358747
Reactome: R-HSA-5358749
Reactome: R-HSA-5358751
Reactome: R-HSA-5358752
Reactome: R-HSA-5626467
Reactome: R-HSA-8853884
Reactome: R-HSA-8876493
Reactome: R-HSA-8951430
Reactome: R-HSA-9733709
Reactome: R-HSA-9754189
Reactome: R-HSA-9762292
Reactome: R-HSA-9764302
Reactome: R-HSA-9793380
Reactome: R-HSA-9796292
Reactome: R-HSA-9823730
Reactome: R-HSA-9824272
Reactome: R-HSA-9833576
Cellular Localisation Cytoplasm
Nucleus
Cytoskeleton
Cell Junction
Adherens Junction
Cell Membrane
Microtubule Organizing Center
Centrosome
Spindle Pole
Synapse
Cilium Basal Body
Colocalized With Rapgef2 And Tjp1 At Cell-Cell Contacts
Cytoplasmic When It Is Un-Stable (Highly Phosphorylated) Or Bound To Cdh1
Translocates To The Nucleus When It Is Stabilized (Low Level Of Phosphorylation)
Interaction With Glis2 And Muc1 Promotes Nuclear Translocation
Interaction With Emd Inhibits Nuclear Localization
The Majority Of Beta-Catenin Is Localized To The Cell Membrane
In Interphase
Colocalizes With Crocc Between Cep250 Puncta At The Proximal End Of Centrioles
And This Localization Is Dependent On Crocc And Cep250
In Mitosis
When Nek2 Activity Increases
It Localizes To Centrosomes At Spindle Poles Independent Of Crocc
Colocalizes With Cdk5 In The Cell-Cell Contacts And Plasma Membrane Of Undifferentiated And Differentiated Neuroblastoma Cells
Interaction With Fam53b Promotes Translocation To The Nucleus
Alternative Protein Names Catenin Beta-1 protein
Beta-Catenin protein
CTNNB1 protein
CTNNB protein
OK protein
SW-cl.35 protein
PRO2286 protein

Information sourced from Uniprot.org

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