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The protein encoded by PTP4A1 belongs to a small class of prenylated protein tyrosine phosphatases (PTPs), which contains a PTP domain and a characteristic C-terminal prenylation motif. Additionally we are shipping PTP4A1 Antibodies (102) and PTP4A1 Proteins (10) and many more products for this protein.
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data shed new light on the structural basis underlying the interaction between PRL (show PRL ELISA Kits) phosphatases and CNNM transporters and provides a hypothesis about the molecular mechanism by which PRL-1, upon binding to CNNM2, might increase the intracellular concentration of Mg(2 (show MCOLN1 ELISA Kits)+) thereby contributing to tumor progression and metastasis.
Prl-1 is required for proper timing of liver regeneration after partial hepatectomy
PRL-1 binding to p115 RhoGAP provides a coordinated mechanism underlying ERK1/2 (show MAPK1/3 ELISA Kits) and RhoA (show RHOA ELISA Kits) activation
In cones and cone-derived cultured cells both Prl-1 activity and Prl-1 gene expression are modulated under oxidative stress.
PTP4A1 is a direct downstream target of miR (show MLXIP ELISA Kits)-1271 in the hepatocellular carcinoma.
PTP4A1 is highly expressed in fibroblasts from patients with systemic sclerosis and enhances pro-fibrotic TGFbeta (show TGFB1 ELISA Kits) signaling in these cells.
PTP4A1 was overexpressed in ICC and played an important role in the progression and metastasis of ICC. The functional role of PTP4A1 was assumed to be acted by activation PI3K (show PIK3CA ELISA Kits)/AKT (show AKT1 ELISA Kits) signaling and promoting the EMT (show ITK ELISA Kits) process through two pivotal transcriptional factors Zeb1 (show ZEB1 ELISA Kits) and Snail (show SNAI1 ELISA Kits).
Results showed that SIAH1 (show SIAH1 ELISA Kits) and PTP4A1 expression was regulated by mir (show MLXIP ELISA Kits)-944 in breast cancer cells. miR (show MLXIP ELISA Kits)-944 binds directly the 3 UTR (show UTS2R ELISA Kits) of their promotor region.
miR (show MLXIP ELISA Kits)-601 inhibits growth and invasion of breast cancer cells by targeting PTP4A1.
Data indicate that protein-tyrosine-phosphatase of regenerating liver 1 (PRL1) gene was expressed much more highly in prostate cancer (PCa) than in nonneoplastic prostate samples.
Upregulation of PRL-1 expression is inversely correlated with miR (show MLXIP ELISA Kits)-26a in primary cervical cancer tissues.
Data highlight the oncogenic function of PRL-1 in HCC invasion and metastasis.
We confirmed with our previous findings that PTP4A1-PHF3-EYS variants were significantly associated with alcohol dependence.
PTP4A1-PHF3-EYS variants were associated with alcohol dependence.
The protein encoded by this gene belongs to a small class of prenylated protein tyrosine phosphatases (PTPs), which contains a PTP domain and a characteristic C-terminal prenylation motif. PTPs are cell signaling molecules that play regulatory roles in a variety of cellular processes. This tyrosine phosphatase is a nuclear protein, but may primarily associate with plasma membrane. The surface membrane association of this protein depends on its C-terminal prenylation. Overexpression of this gene in mammalian cells conferred a transformed phenotype, which implicated its role in the tumorigenesis. Studies in rat suggested that this gene may be an immediate-early gene in mitogen-stimulated cells.
protein tyrosine phosphatase type IVA 1
, protein tyrosine phosphatase type IVA, member 1
, Protein tyrosine phosphatase type IVA 1
, protein-tyrosine phosphatase 4a1
, protein-tyrosine phosphatase of regenerating liver 1
, protein tyrosine phosphatase type IVA protein 1
, protein tyrosine phosphatase 4a1