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anti-R-PTP-rho, mAb (T20-AF3C7)
Product Details | |
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Synonyms | PTPRT; R-PTP-T; RPTP-ρ; KIAA0283; EC=3.1.3.48; Receptor-type Tyrosine-Protein Phosphatase T; Receptor-type Tyrosine-Protein Phosphatase ρ |
Product Type | Monoclonal Antibody |
Properties | |
Clone | T20-AF3C7 |
Isotype | Mouse IgG1 κ |
Immunogen/Antigen | Recombinant human protein purified from E. coli. |
Application |
Western Blot (1:5,000) |
Crossreactivity | Human |
Purity Detail | Ammonium sulfate precipitation. |
Formulation | Liquid. HEPES with 0.15M NaCl, 0.01% BSA, 0.03% sodium azide, and 50% glycerol. |
Isotype Negative Control | |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
Declaration | Manufactured by AbFrontier |
Shipping and Handling | |
Shipping | BLUE ICE |
Short Term Storage | +4°C |
Long Term Storage | -20°C |
Use/Stability | Stable for at least 1 year after receipt when stored at -20°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet |
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Receptor protein tyrosine phosphatase rho (RPTPρ/PTPRT) is a transmembrane protein that is highly expressed in the developing and adult central nervous system. It is a member of the RPTP R2B subfamily, which includes PTPκ, PTPμ and PCP-2. The R2B phosphatases are known to interact with members of the cadherin/catenin complex. These four RPTPs share the same domain structure: an extracelluar domain, a juxtamembrane region, and two phosphatase domains. The extracellular domain of PTPR mediates cell-cell aggregation and that mutational inactivation of this phosphatase could promote tumor migration and metastasis. PTPRT is the most frequently mutated PTP in human cancers. STAT3 is a substrate of PTPRT. Phosphorylation of a tyrosine at 705 is essential for the function of STAT3, and PTPRT specifically dephosphorylated STAT3 at this position. May be involved in both signal transduction and cellular adhesion in the CNS.
1) Yu J et al., (2008) Mol Cancer Res 6(7):1106-13. (General)
2) Zhang X et al., (2007) Proc Natl Acad Sci 104(10):4060-4. (General)
3) Besco JA et al., (2006) Brain Res 1116(1):50-7. (General)