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- rabbit polyclonal IgG, 200 µg/ml
- epitope mapping at the C-terminus of FGFR-3 of human origin
- recommended for detection of FGFR-3 of mouse, rat and human origin by WB, IP, IF, IHC(P) and ELISA
- blocking peptide, sc-123 P
- agarose conjugate for IP studies, sc-123 AC, 500 µg/0.25 ml agarose
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FGFR-3 Background Information Acidic and basic fibroblast growth factors (FGFs) are members of a family of multifunctional polypeptide growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin (1). Like other growth factors, FGFs act by binding and activating specific cell surface receptors. These include the Flg receptor or FGFR-1, the Bek receptor or FGFR-2, FGFR-3, FGFR-4, FGFR-5 and FGFR-6 (2). These receptors usually contain an extracellular ligand-binding region containing three immunoglobulin-like domains, a transmembrane domain and a cytoplasmic tyrosine kinase domain (3,4). The gene encoding human FGFR-3 maps to chromosome 4p16 and is alternatively spliced to produce three isoforms that are expressed in brain, kidney and testis (5,6). Defects in FGFR-3 are associated with several diseases, including Crouzon syndrome, achondroplasia, thanatophoric dysplasia, craniosynostosis adelaide type and hypochondroplasia (7–10). Mutations in FGFR-3 are also a cause of some bladder and cervical cancers (11).
| FGFR-3 (C-15) Product Citations |
See how others have used FGFR-3 (C-15): sc-123 antibody and or FGFR-3 (C-15) antibody conjugates.
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FGFR-3 (C-15)
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FGFR-3 (C-15): sc-123. Western blot analysis of FGFR-3 expression in A549 (A) and T-47D (B) whole cell lysates.
Immunoperoxidase staining of formalin-fixed, paraffin-embedded rat cranial suture (A), human calvarium (B) and human skin (C). Antibodies tested include Bek (C-17): sc-122 (A), FGFR-3 (C-15): sc-123 (B) and FGFR-4 (C-16): sc-124 (C). Kindly provided by Leslie Gold.
FGFR-3 (C-15): sc-123. Immunoperoxidase staining of formalin fixed, paraffin-embedded human colon tissue showing cytoplasmic staining of smooth muscle cells.
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