Phospho-Shp2 (Tyr580) (4A2) rabbit mAb

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SKU
2101
Src homology region 2 (SH2)-containing protein tyrosine phosphatase 2 (Shp2, phospho Shp2), encoded by PTPN11 gene, is a non-receptor phosphotyrosine phosphatase which is ubiquitously expressed in mammalian cells and contain one protein tyrosine phosphatase (PTP) catalytic domain and two SH2 domains. The phosphatase active site is located in the C-terminal of Shp2. Shp2 is phosphorylated by several stimulants and cytokines at Tyr580 inducing Shp2 activation. Activated Shp2 recruits Grb2 and Tyr580 phosphorylation of phospho Shp2 functions as the main binding site of Grb2, thereby activating downstream Ras in response to growth factors. In turn Grb2 controls FGFR2 phosphorylation by inhibiting receptor kinase and Shp2 phosphatase activity. Shp2 also promotes both ERK1/2 and PI3K/AKT signaling. High levels of Shp2 has been found in several cancer types including breast cancer and melanoma.
More Information
Applications Flow Cytometry
Clone Shp2Y580-4A2
Format Unconjugated
Validated Reactivity Human, Mouse
Cross Reactivity Predicted to work with mouse, rat and other homologues.
Detection Anti-Rabbit IgG
Clonality Monoclonal
Immunogen A synthetic phospho-peptide corresponding to residues surrounding Tyr580 of human phospho Shp2
Formulation 1X PBS, 0.02% NaN3, 50% Glycerol, 0.1% BSA
Isotype Rabbit IgGk
Preparation Protein A+G
Recommended Usage 1µg/mL – 0.001µg/mL. It is recommended that the reagent be titrated for optimal performance for each application. See product image legends for additional information.
Storage -20ºC
Pseudonyms Tyrosine-protein phosphatase non-receptor type 11, Protein-tyrosine phosphatase 1D, PTP-1D, Protein-tyrosine phosphatase 2C, SH-PTP3, PTPN11, PTP2C, SHPTP2
Uniprot ID Q06124
References 1. Bennett AM et al., (1994) Proc Natl Acad Sci USA. 91:7335–9. 2. Feng GS et al., (1994) Trends Genet. 10:54–8. 3. Mohi MG et al., (2007) Curr Opin Genet Dev. 17:23–30. 4. Vogel W et al., (1996) Cell Growth Differ. 7:1589–97 5. Ahmed Z et al., (2013) J Cell Biol. 200:493–504. 6. Hu ZQ et al., (2014) Oncol Rep 32:205-212.
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