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貨期:
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用途:
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Protein tyrosine phosphatase which stimulates progression from G1 into S phase during mitosis. May play a role in the development and maintenance of differentiating epithelial tissues. Enhances cell proliferation, cell motility and invasive activity, and promotes cancer metastasis.
基因功能參考文獻:
PTP4A1 is a direct downstream target of miR-1271 in the hepatocellular carcinoma. PMID: 29345291
PTP4A1 is highly expressed in fibroblasts from patients with systemic sclerosis and enhances pro-fibrotic TGFbeta signaling in these cells. PMID: 29057934
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/AKT signaling and promoting the EMT process through two pivotal transcriptional factors Zeb1 and Snail. PMID: 27655691
Results showed that SIAH1 and PTP4A1 expression was regulated by mir-944 in breast cancer cells. miR-944 binds directly the 3 UTR of their promotor region. PMID: 27377268
miR-601 inhibits growth and invasion of breast cancer cells by targeting PTP4A1. PMID: 27044835
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. PMID: 24968948
Upregulation of PRL-1 expression is inversely correlated with miR-26a in primary cervical cancer tissues. PMID: 24939702
Data highlight the oncogenic function of PRL-1 in HCC invasion and metastasis. PMID: 25003523
We confirmed with our previous findings that PTP4A1-PHF3-EYS variants were significantly associated with alcohol dependence. PMID: 24961364
PTP4A1-PHF3-EYS variants were associated with alcohol dependence. PMID: 23324950
Results suggest that TRP32 maintains the reduced state of PRL and thus regulates the biological function of PRL. PMID: 23362275
Studies indicate that PRL-1 and PRL-2 and PRL-3 are oncogenes and belong to the few phosphatases that lead to the development of cancer. PMID: 22413991
upregulation of PRL-1 protein correlates with shortened patient survival in human hepatocellular carcinoma PMID: 22484636
Data conclude that the PHF3-PTP4A1 region appears to harbor a causal locus for alcohol dependence, and proteins encoded by PHF3 and/or PTP4A1 might play a functional role in the disorder. PMID: 22096494
PRL-1 binding to p115 RhoGAP provides a coordinated mechanism underlying ERK1/2 and RhoA activation PMID: 22009749
Increased PRL1 expression results in activation of Src and ERK1/2, which stimulates MMP2 and MMP9 production, leading to increased cell migration and invasion. PMID: 19199380
PRL-1 function is regulated in a cell cycle-dependent manner and implicate PRL-1 in regulating progression through mitosis, possibly by modulating spindle dynamics PMID: 12235145
PRL phosphatases increase cell proliferation by stimulating progression from G1 into S phase PMID: 14643450
PRL-1 phosphatase has a trimeric structure which reveals an active enzyme conformation and regulation mechanisms PMID: 15571731
PRL-1 mRNA expression was not significantly higher in malignant compared to benign breast tissue. PMID: 16832410
PRL-1 expression levels varied considerably both between tissue types and cell type examined. Widespread expression of PRL-1 in multiple organ systems suggests an important functional role for these enzymes in normal tissue homeostasis. PMID: 16957164
Colonic adenocarcinoma cells have the ability to produce PTP4A1, PTP4a2, and PTP4A3, which may relate to the lymph node metastasis of colonic adenocarcinoma. PMID: 17440740
that trimerization may be a general property for all PRL enzymes, and that PRL1 trimer formation is essential for the PRL1-mediated cell growth and migration. PMID: 17656357
PRL-1 and PRL-3 mRNAs may be involved in and used to predict the metastasis of esophageal squamous cell carcinoma. Possibility of using PRL-1 and PRL-3 as therapeutical target. PMID: 18684031
the new oncogenic p53 target, PRL-1, may contribute to tumor development by the downregulation of p53 by a negative feedback mechanism. PMID: 18997816
phosphatase of regenerating liver activity is controlled by the redox environment and its C-terminal residues PMID: 19341304