Recombinant Rat Tyrosine-protein phosphatase non-receptor type 1 (Ptpn1)

Product Details

Purity
>85% (SDS-PAGE)
Target Names
Ptpn1
Uniprot NO.
Alternative Names
Ptpn1; Tyrosine-protein phosphatase non-receptor type 1; EC 3.1.3.48; Protein-tyrosine phosphatase 1B; PTP-1B
Species
Rattus norvegicus (Rat)
Source
Yeast
Expression Region
1-432
Target Protein Sequence
MEMEKEFEQI DKAGNWAAIY QDIRHEASDF PCRIAKLPKN KNRNRYRDVS PFDHSRIKLH QEDNDYINAS LIKMEEAQRS YILTQGPLPN TCGHFWEMVW EQKSRGVVML NRIMEKGSLK CAQYWPQKEE KEMVFDDTNL KLTLISEDVK SYYTVRQLEL ENLATQEARE ILHFHYTTWP DFGVPESPAS FLNFLFKVRE SGSLSPEHGP IVVHCSAGIG RSGTFCLADT CLLLMDKRKD PSSVDIKKVL LEMRRFRMGL IQTADQLRFS YLAVIEGAKF IMGDSSVQDQ WKELSHEDLE PPPEHVPPPP RPPKRTLEPH NGKCKELFSN HQWVSEESCE DEDILAREES RAPSIAVHSM SSMSQDTEVR KRMVGGGLQS AQASVPTEEE LSPTEEEQKA HRPVHWKPFL VNVCMATALA TGAYLCYRVC FH
Note: The complete sequence may include tag sequence, target protein sequence, linker sequence and extra sequence that is translated with the protein sequence for the purpose(s) of secretion, stability, solubility, etc.
If the exact amino acid sequence of this recombinant protein is critical to your application, please explicitly request the full and complete sequence of this protein before ordering.
Protein Length
Full length protein
Tag Info
N-terminal His-tagged/Tag-Free
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
Storage Condition
Store at -20°C, for extended storage, conserve at -20°C or -80°C.
Shelf Life
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
Notes
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.

Customer Reviews and Q&A

 Customer Reviews

Target Background

Function(From Uniprot)
Tyrosine-protein phosphatase which acts as a regulator of endoplasmic reticulum unfolded protein response. Mediates dephosphorylation of EIF2AK3/PERK; inactivating the protein kinase activity of EIF2AK3/PERK. May play an important role in CKII- and p60c-src-induced signal transduction cascades. May regulate the EFNA5-EPHA3 signaling pathway which modulates cell reorganization and cell-cell repulsion. May also regulate the hepatocyte growth factor receptor signaling pathway through dephosphorylation of MET.
Gene References into Functions
  1. These findings reveal a novel role for pancreatic PTP1B in cerulein- and arginine-induced acute pancreatitis. PMID:27461362
  2. deleterious role that the amygdalar PTP1B has on energy homeostasis in obesity states PMID:28403933
  3. The results suggest that neonatal MS experience may blunt the anorectic efficacy of leptin later in life, possibly in relation with increased expressions of PTP1B and/or pSTAT3 in the hypothalamus PMID:28229972
  4. overexpression of PTP1B can inhibit glucose-stimulated insulin secretion in INS-1 cells through negatively regulating insulin signaling. PMID:26099503
  5. PTP1B expression is up-regulated following spinal cord injury. PMID:25894283
  6. Study suggested that brain mitochondrial dysfunction following lipopolysaccharide-induced sepsis in rats is partly attributed to PTP1B and Src mediated decrease in mitochondrial protein tyrosine phosphorylation PMID:25998537
  7. After retinal detachment, weak immunolabeling of PTP1B was seen in the retinal pigment epithelial cells. PMID:25999679
  8. Overexpression of PTP1B by treatment with free fatty acids did not translate into negative modulation of insulin signaling in cells treated with unsaturated free fatty acids. PMID:23481236
  9. Complement-mediated glomerular injury is reduced by inhibition of protein-tyrosine phosphatase 1B. PMID:25056348
  10. An increased PTP1B expression in the hypothalamus underlies the development of leptin resistance during repeated exposure to Lipopolysaccharides. PMID:25352433
  11. Data indicate that protein tyrosine phosphatases SHP-1, SHP-2 and PTP1B overexpressed during the development of cerulein -induced acute pancreatitis can be modulated by extracellular signal-regulated kinases (ERK1/2) and c-Jun NH2-terminal kinase (JNK). PMID:24225419
  12. Contents released from injured epithelial cells can inactivate renal fibroblasts by dephosphorylation of EGFR through a mechanism involved in PTP1B activation. PMID:23283996
  13. role of PTP1B in structural plasticity within the hippocampus PMID:22844492
  14. Fe(2+)-generated O(2) mediates p21(ras) and TAK1 activation via PTP inhibition and Lys(63)-polyUb of TRAF6 in caveosomes for proinflammatory M1 activation in hepatic macrophages PMID:22829592
  15. PTP1b within the solitary tract nucleus may be a novel molecular mechanism for preservation of resting baroreflex function and provides further evidence for deleterious cardiovascular effects associated with PTP1b inhibition PMID:22569287
  16. The data suggest that TNFalpha acts on the hypothalamus to increase hypothalamic PTP1B expression and activity via the NFkappaB pathway PMID:22166493
  17. The regulatory function of Src and its modulation by PTP1B on oxidative phosphorylation in mitochondria. PMID:21063895
  18. the upregulation of PTP1B by platelet-derived growth factor or nitric oxide is both necessary and sufficient to induce the downregulation of protein kinase G via an effect on PKG mRNA levels. PMID:21057040
  19. results indicate that activation of PTP1B in the liver could induce hypertriglyceridaemia and that anchoring of PTP1B to the membrane is crucial for its action PMID:19605464
  20. results demonstrated that the increase in protein tyrosine phosphatase 1B expression and/or association with insulin receptor in monosodium glutamate animals may contribute to the impaired insulin signaling mainly in liver and muscle PMID:12850498
  21. PTP1B, best known as a negative regulator of the metabolic effects of insulin, is required for the effects of insulin on actin organization in immortalized fibroblasts PMID:12902327
  22. Protein-tyrosine phosphatase 1B is a new activator for hepatic lipogenesis via sterol regulatory element-binding protein-1 gene expression PMID:12941932
  23. Vascular injury induced by balloon catheter increases levels. These effects occur in PTP specific, as well as temporally and regionally specific, manner. PMID:15271661
  24. existence of an inhibitory feedback loop involving PDGF or FGF, and PTP1B in blood vessels PMID:16373608
  25. The catalytic domain of rat recombinant protein tyrosine phosphatase eta has been produced in Escherichia coli in soluble form, crystallized, and purified to homogeneity. PMID:16946481
  26. Diet-induced obesity increased expression and activity of the protein tyrosine phosphatase 1B and attenuated insulin signalling in gastrocnemius muscle of rats, which was reversed by single session of exercise. PMID:17008371
  27. increases in PTP1B contribute to hypothalamic leptin resistance as rats transition into middle age PMID:17038557
  28. PTP1B plays a role in the negative regulation of EGF-induced signaling and helps suppress cell cycle entry. PMID:17563729
  29. PTP1B overexpression in multiple tissues in obesity is regulated by inflammation PMID:18281274
  30. Chronic insulin treatment amplifies PDGF-BB induced motility in differentiated aortic smooth muscle cells by suppressing the expression and function of PTP1B. PMID:18456732
  31. Somatostatin receptors 1, 2, and 5 cooperate in the somatostatin inhibition of C6 glioma cell proliferation in vitro via a phosphotyrosine phosphatase-eta-dependent inhibition of extracellularly regulated kinase-1/2. PMID:18566118
  32. Localization of PTP-1B, SHP-2, and Src exclusively in rat brain mitochondria and functional consequences.( PMID:18583343

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Subcellular Location
Endoplasmic reticulum membrane; Peripheral membrane protein; Cytoplasmic side.
Protein Families
Protein-tyrosine phosphatase family, Non-receptor class 1 subfamily
Tissue Specificity
Found in several tissues including central nervous system, liver and kidney. A high level of expression was found in the hippocampus.
Database Links
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