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Phospho-EphA2-S897 Antibody Blocking PeptideSynthetic peptide
| Country | United States
Ordering Information
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| Catalog # | Size | Availability | Price | |
| BP3722a | 0.1 mg 400 ul | In Stock | $ 45.00 | DISCONTINED INQUIRE CLICK INQUIRE Add to cart |
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- Citiations : 0
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Phospho-EphA2-S897 Antibody Blocking Peptide - Product info | |
| Primary Accession | P29317 |
| Calculated MW | 108266 Da |
Phospho-EphA2-S897 Antibody Blocking Peptide - Additional info | |
| Gene ID 1969 | |
| Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml. | |
| Storage Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. | |
| Precautions This product is for research use only. Not for use in diagnostic or therapeutic procedures. | |
Phospho-EphA2-S897 Antibody Blocking Peptide - Protein Information | |
| Name EPHA2 | |
| Synonyms ECK | |
| Function Receptor tyrosine kinase which binds promiscuously membrane-bound ephrin-A family ligands residing on adjacent cells, leading to contact-dependent bidirectional signaling into neighboring cells. The signaling pathway downstream of the receptor is referred to as forward signaling while the signaling pathway downstream of the ephrin ligand is referred to as reverse signaling. Activated by the ligand ephrin-A1/EFNA1 regulates migration, integrin-mediated adhesion, proliferation and differentiation of cells. Regulates cell adhesion and differentiation through DSG1/desmoglein-1 and inhibition of the ERK1/ERK2 (MAPK3/MAPK1, respectively) signaling pathway. May also participate in UV radiation-induced apoptosis and have a ligand- independent stimulatory effect on chemotactic cell migration During development, may function in distinctive aspects of pattern formation and subsequently in development of several fetal tissues. Involved for instance in angiogenesis, in early hindbrain development and epithelial proliferation and branching morphogenesis during mammary gland development. Engaged by the ligand ephrin-A5/EFNA5 may regulate lens fiber cells shape and interactions and be important for lens transparency development and maintenance. With ephrin-A2/EFNA2 may play a role in bone remodeling through regulation of osteoclastogenesis and osteoblastogenesis | |
| Cellular Location Cell membrane; Single-pass type I membrane protein. Cell projection, ruffle membrane; Single-pass type I membrane protein. Cell projection, lamellipodium membrane; Single- pass type I membrane protein. Cell junction, focal adhesion Note=Present at regions of cell-cell contacts but also at the leading edge of migrating cells | |
| Tissue Location Expressed in brain and glioma tissue and glioma cell lines (at protein level). Expressed most highly in tissues that contain a high proportion of epithelial cells, e.g skin, intestine, lung, and ovary | |
Phospho-EphA2-S897 Antibody Blocking Peptide - Related products
AP3722a: Phospho-EphA2- S897 Antibody
AP7607a: EphA2 Antibody (N-term)
AP7607b: EphA2 Antibody (C-term)
RI11796: EPHA2 predesign siRNA
BP3722a: Phospho-EphA2-S897 Antibody Blocking Peptide
BP7607a: EphA2 Antibody (N-term) Blocking Peptide
BP7607b: EphA2 Antibody (C-term) Blocking Peptide
Phospho-EphA2-S897 Antibody Blocking Peptide - Research Areas
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BACKGROUND
EphA2 belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands.
REFERENCES
Larsen, A.B., et al. Cell. Signal. 22(4):636-644(2010)Salaita, K., et al. Science 327(5971):1380-1385(2010)Zhuang, G., et al. Cancer Res. 70(1):299-308(2010)