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The protein encoded by PTP4A3 belongs to a small class of prenylated protein tyrosine phosphatases (PTPs). De plus, nous expédions PTP4A3 Protéines (11) et PTP4A3 Kits (6) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 76 products:
Human Polyclonal PTP4A3 Primary Antibody pour ELISA, WB - ABIN257782
Fagerli, Holt, Holien, Vaatsveen, Zhan, Egeberg, Barlogie, Waage, Aarset, Dai, Shaughnessy, Sundan, Børset: Overexpression and involvement in migration by the metastasis-associated phosphatase PRL-3 in human myeloma cells. dans Blood 2008
Show all 2 Pubmed References
Human Polyclonal PTP4A3 Primary Antibody pour ELISA, WB - ABIN564844
Fromont, Godet, Peyret, Irani, Celhay, Rozet, Cathelineau, Cussenot: 8q24 amplification is associated with Myc expression and prostate cancer progression and is an independent predictor of recurrence after radical prostatectomy. dans Human pathology 2013
We conclude that PRL-3 is an important regulatory factor for breast cancer cell proliferation and invasion. Loss of PRL-3 function induces an antimetastatic gene expression profile in breast cancer cells. Due to its role in tumor growth and metastasis, PRL-3 emerges as a new therapeutic target in breast cancer therapy.
Since high PRL-3 expression also correlates with poor prognosis in other cancers and functional studies in PC support these findings, PRL-3 emerges as a potential treatment target in PC
Data show that phosphatase of regenerating liver-3 (PRL (Montrer PRL Anticorps)-3a) is an important mediator of growth factor signaling in MM cells and hence possibly a good target for treatment of MM.
Data suggest that phosphatase of regenerating liver-3 (PRL-3)might play a tumor suppressor role in lung cancer, distinct from other cancers, by inhibiting epithelial-mesenchymal transition (EMT (Montrer ITK Anticorps))-related pathways.
A novel role of PRL-3 in tumor development through its adverse impact on telomere homeostasis.
our result indicated that PRL-3 promotes protein phosphorylation by acting as an 'activator kinase' and consequently regulates cytokine secretion.
The disruption of epithelial architecture by PRL-3 revealed here is a newly recognized mechanism for PRL-3-promoted cancer progression.
This study suggests PRL-3 and SFKs are key mediators of the IL6 (Montrer IL6 Anticorps)-driven signaling events.
Regulation of PTP4A3 expression is altered in specific subgroups of acute leukemias and this is likely brought about by expression of the aberrant ETV6 (Montrer ETV6 Anticorps)-RUNX1 (Montrer RUNX1 Anticorps) and BCR (Montrer BCR Anticorps)-ABL1 (Montrer ABL1 Anticorps) fusion genes.
PRL-3 engages the focal adhesion pathway in trip0le-negative breast cancer cells as a key mechanism for promoting TNBC cell migration and invasion.
Results uncovered that aberrant overexpression of PRL-3 could initiate chordoma in early development.
Data show that protein-tyrosine phosphatase (Montrer ACP1 Anticorps) PRP4A3 (prl3) and van gogh like1 (vangl1 (Montrer Vangl1 Anticorps)) are Necessary Components in prohibitin1 (phb1 (Montrer PHB Anticorps)) dependent neural crest specification.
PTP4A3 is required for cephalic neural crest migration in vivo during embryonic development.
our results suggest that the Prl3b1-cre mice line provides a unique resource to understand testicular germ-cell development
Results demonstrate that Ptp4a3 contributes to the malignant phenotype of tumor-initiating cells.
PRL-3 protein was significantly reduced in mouse STAT3 (Montrer STAT3 Anticorps)-knockout liver cells compared with STAT3 (Montrer STAT3 Anticorps)-wild type counterparts, and ectopic expression of STAT3 (Montrer STAT3 Anticorps) in these cells led to a pronounced increase in PRL-3 protein.
Data indicate that Mycobacterium tuberculosis T cell stimulatory epitope (MT) is a potentially effective molecular adjuvant in preparation of monoclonal antibody (mAb) specific for phosphatase of regenerating liver-3 (PRL-3).
These findings strongly support a role for PTP4A3 as an important contributor to endothelial cell function and as a multimodal target for cancer therapy and mitigating VEGF (Montrer VEGFA Anticorps)-regulated angiogenesis.
the first definitive evidence implicating Ptp4a3 in colon tumorigenesis
role of PTP4A3 in acute myeloid leukemia (Montrer BCL11A Anticorps)
PTP4A3 was identified as a novel negative regulator of LPS (Montrer TLR4 Anticorps)-induced LITAF/TNF-alpha production.
PRL-3 was highly expressed in metastatic melanoma B16-BL6 cells but not in its lowly metastatic parental cell line, B16 cells
PRL-3-expressing cells rapidly induce metastatic tumor formation in lung
The protein encoded by this gene belongs to a small class of prenylated protein tyrosine phosphatases (PTPs). PTPs are cell signaling molecules that play regulatory roles in a variety of cellular processes. This class of PTPs contain a PTP domain and a characteristic C-terminal prenylation motif. Studies of this class of PTPs in mice demonstrated that they were prenylated proteins in vivo, which suggested their association with cell plasma membrane. Overexpression of this gene in mammalian cells was reported to inhibit angiotensin-II induced cell calcium mobilization and promote cell growth. Two alternatively spliced variants exist.
potentially prenylated protein tyrosine phosphatase
, protein tyrosine phosphatase type IVA 3
, protein-tyrosine phosphatase 4a3
, protein-tyrosine phosphatase of regenerating liver 3
, protein tyrosine phosphatase type IVA, member 3
, protein tyrosine phosphatase 4a3