| Code | CSB-MP008646HU1(F2) |
| Abbreviation | Recombinant Human FGFR3 protein, partial (Active) |
| MSDS | |
| Size | $114 |
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FGFR3 dysregulation drives oncogenesis in bladder carcinoma, multiple myeloma, and thanatophoric dysplasia, making validated extracellular domain constructs essential tools for dissecting ligand-receptor interactions and screening therapeutic candidates. This mammalian-expressed construct spanning residues 23–377 of isoform 2 captures the complete ligand-binding region and demonstrates quantifiable antibody-binding activity with an EC50 of 0.72–1.53 ng/mL in functional ELISA, providing a reliable basis for competitive inhibition assays, blocking antibody screening, and therapeutic antibody epitope mapping. The measured affinity supports its use as a positive control in SPR and BLI experiments characterizing anti-FGFR3 biologics or small-molecule inhibitors targeting the extracellular interface. Purity exceeding 95% by SDS-PAGE and endotoxin levels below 1.0 EU/μg align with standards expected in high-sensitivity binding platforms and cell-based receptor occupancy studies.
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