mProX™ Human EPHA3 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Inducible EPHA3 overexpression in colon cancer cell lines.
Western blot shows LS174T and DLD1 cells that were transfected with pLenti/TO-EPHA3 or the control empty vector (EV) and treated with the appropriate doxycycline doses for 48 hours, demonstrating the amounts of EPHA3 protein in the cells.
Ref: Andretta, Elena, et al. "Investigation of the role of tyrosine kinase receptor EPHA3 in colorectal cancer." Scientific reports 7.1 (2017): 41576.
Pubmed: 28169277
DOI: 10.1038/srep41576
Research Highlights
The transmembrane glycoprotein members of the tyrosine kinase receptor family are the erythropoietin-producing human hepatocellular (Eph) receptors. The phosphorylation of their tyrosine kinase domain and the activation of the Eph receptor are the outcomes of the Ephs binding to different ephrin ligands.
London, Max, and Eugenio Gallo. "Critical role of EphA3 in cancer and current state of EphA3 drug therapeutics." Molecular Biology Reports 47 (2020): 5523-5533.
Pubmed:
32621117
DOI:
10.1007/s11033-020-05571-8
By binding and activating both human and mouse EphA3, the EphA3-specific monoclonal antibody (mAb), IIIA4, was able to identify the human EphA3 gene in a pre-B acute lymphoblastic leukemia (pre-B-ALL).
Charmsaz, Sara, et al. "EphA3 as a target for antibody immunotherapy in acute lymphoblastic leukemia." Leukemia 31.8 (2017): 1779-1787.
Pubmed:
27922598
DOI:
10.1038/leu.2016.371