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The protein encoded by CTNNBIP1 binds CTNNB1 and prevents interaction between CTNNB1 and TCF family members. Additionally we are shipping CTNNBIP1 Antibodies (49) and CTNNBIP1 Kits (5) and many more products for this protein.
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miR (show MLXIP Proteins)-215-5p is a negative regulator of adipocyte differentiation through post-transcriptional regulation of FNDC3B and CTNNBIP1 during early adipogenesis
miR (show MLXIP Proteins)-29b plays a pivotal role in fetal mouse neurogenesis by regulating ICAT-mediated Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling.
Mechanistic studies revealed that CTNNBIP1 suppresses Wnt (show WNT2 Proteins)/beta-catenin (show CTNNB1 Proteins) signaling and that miR (show MLXIP Proteins)-215 promotes beta-catenin (show CTNNB1 Proteins) activation and upregulates alpha-SMA (show SMN1 Proteins) and fibronectin (show FN1 Proteins) expression in TGF-beta1 (show TGFB1 Proteins)-treated MMCs by targeting CTNNBIP1
Overexpression of Icat induces G(2) arrest and cell death in tumor cell mutants for adenomatous polyposis coli (show APC Proteins), beta-catenin (show CTNNB1 Proteins), or Axin (show AXIN1 Proteins).
ICAT plays an important role in the anteriorization of neural cells by inhibiting the posteriorizing activity of Wnt (show WNT2 Proteins) signaling
These results suggest that the loss of ICAT gene function causes the arrest of UB branching and the apoptotic death of MM cells, resulting in renal agenesis.
Inhibition of beta-catenin (show CTNNB1 Proteins) signaling in articular chondrocytes causes increased cell apoptosis and articular cartilage destruction in Col2a1 (show COL2A1 Proteins)-ICAT- transgenic mice.
Data demonstrated that ICAT was highly expressed in cervical cancer tissues and had a role in control of epithelial-mesenchymal transition (EMT) in cervical cancer cells. Its overexpression promoted cell proliferation, migration, invasion and resulted in EMT by disrupting the stability of E-cadherin/betacatenin complex.
Low PLD1 expression and high ICAT expression were significantly associated with increased survival in colorectal cancer patients.
The present work aims to investigate the relationship between the expression of AEG-1 (show MTDH Proteins)(astrocyte elevated gene-1), b-FGF(basic-fibroblast growth factor (show FGF2 Proteins)), beta-catenin (show CTNNB1 Proteins), Ki-67 (show MKI67 Proteins), TNF-alpha (tumor necrosis factor (show TNF Proteins)-alfa) other prognostic parameters in DC (Ductal Carcinomas) and ductal intraepithelial neoplasm. We found a relationship between these factors.
Overexpression of ICAT promoted Caski cells' proliferation, arrested the cell cycle in the S phase and enhanced cell migration. Conclusion Overexpression of ICAT can promote the proliferation and migration of Caski cervical cancer cells.
Somatic mutation of beta-catenin (CTNNB1 (show CTNNB1 Proteins)) is known to be crucial for Wilms tumor development in up to 15% of cases.
CTNNBIP1 expression correlated with longer overall survival in LAC (show LCT Proteins) patients. This study reveals that miR (show MLXIP Proteins)-214 plays a critical role in CSLC self-renewal and stemness by targeting CTNNBIP1.
Data show that microRNA miR (show MLXIP Proteins)-215 activates beta-catenin (show CTNNB1 Proteins) pathways by decreasing catenin beta interacting protein 1 (CTNNBIP1)expression in gliomas.
Simultaneous silencing of beta-catenin (show CTNNB1 Proteins) and STAT3 (show STAT3 Proteins) synergistically induces apoptosis and inhibits cell proliferation in HepG2 liver cancer cells.
Finally, pro-incubation with idebenone inhibited mitochondrial dysfunction induced by oxLDL through the mitochondrial-dependent apoptotic pathway and GSK3beta/beta-catenin (show CTNNB1 Proteins) signalling pathways.
A potent beta-catenin (show CTNNB1 Proteins) inhibitor, ICAT/CTNNBIP1 was a direct target of miR (show MLXIP Proteins)-424-5p.
The protein encoded by this gene binds CTNNB1 and prevents interaction between CTNNB1 and TCF family members. The encoded protein is a negative regulator of the Wnt signaling pathway. Two transcript variants encoding the same protein have been found for this gene.
, beta-catenin-interacting protein 1
, catenin, beta interacting protein 1 a
, catenin beta interacting protein 1 b
, catenin, beta interacting protein 1
, inhibitor of beta-catenin and Tcf-4
, beta-catenin-interacting protein ICAT