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FGFR3 Protein (Soluble)

FGFR3 Origin: Human Host: Insect Cells Recombinant > 95 % by SDS-PAGE
Catalog No. ABIN7539328
  • Target See all FGFR3 Proteins
    FGFR3 (Fibroblast Growth Factor Receptor 3 (FGFR3))
    Protein Type
    Recombinant
    Protein Characteristics
    Soluble
    Origin
    • 20
    • 4
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 7
    • 7
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    Insect Cells
    Purpose
    FGFR-3(IIIa), soluble
    Sequence
    ESLGTEQRV VGRAAEVPGP EPGQQEQLVF GSGDAVELSC PPPGGGPMGP TVWVKDGTGL V PSERVLVGP QRLQVLNASH EDSGAYSCRQ RLTQRVLCHF SVRVTDAPSS GDDEDGEDEA E DTGVDTGAP YWTRPERMDK KLLAVPAANT VRFRCPAAGN PTPSISWLKN GREFRGEHRI G GIKLRHQQW SLVMESVVPS DRGNYTCVVE NKFGSIRQTY TLDVLERSPH RPILQAGLPA N QTAVLGSDV EFHCKVYSDA QPHIQWLKHV EVNGSKVGPD GTPYVTVLKT R
    Specificity
    Chromosomal location:4q16.3
    Characteristics
    Length (aa):290
    Purity
    > 95 % by SDS-PAGE
    Top Product
    Discover our top product FGFR3 Protein
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
  • Target
    FGFR3 (Fibroblast Growth Factor Receptor 3 (FGFR3))
    Alternative Name
    FGFR-3 (FGFR3 Products)
    Synonyms
    FGFR3 Protein, LOC100034114 Protein, ACH Protein, CD333 Protein, CEK2 Protein, HSFGFR3EX Protein, JTK4 Protein, FR3 Protein, Fgfr-3 Protein, Flg-2 Protein, HBGFR Protein, Mfr3 Protein, sam3 Protein, fc27h01 Protein, wu:fc27h01 Protein, fibroblast growth factor receptor 3 Protein, fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism) S homeolog Protein, FGFR3 Protein, fgfr3.S Protein, Fgfr3 Protein, fgfr3 Protein
    Background
    Fibroblast growth factor receptor 3, FGFR-3/ CD333,The Fibroblast growth factor receptors (FGFRs) are a family of receptor tyrosine kinases that play key roles in proliferation, differentiation, and tumorigenesis. The FGFR3(IIIb) isoform was identified as the major family member expressed in normal human urothelium. Already in 2005 a splice variant, FGFR3ΔTM, lacking exons encoding the COOH-terminal half of immunoglobulin-like domain III and the transmembrane domain was described. Previous reports had assumed that this is would be a cancer-specific splice variant but in 2005 it was shown that FGFR3ΔTM is a normal transcript in NHU cells and is translated, N-glycosylated, and secreted. Primary urothelium expressed high levels of FGFR3ΔTM transcripts. In culture, levels were reduced in actively proliferating cells but increased at confluence and as cells approached senescence. Cells overexpressing FGFR3 IIIb showed FGF1-induced proliferation, which was inhibited by the addition of FGFR3ΔTM. In bladder tumor cell lines derived from aggressive carcinomas, there were significant alterations in the relative expression of isoforms including an overall decrease in the proportion of FGFR3ΔTM and predominant expression of FGFR3 IIIc in some cases. In summary, alternative splicing of FGFR3 IIIb in NHU cells represents a normal mechanism to generate a transcript that regulates proliferation and in bladder cancer, the ratio of FGFR3 isoforms is significantly altered.
    Molecular Weight
    31.7 kDa
    Gene ID
    2261
    NCBI Accession
    NM_022965, NP_075254
    UniProt
    P22607-3
    Pathways
    RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Stem Cell Maintenance, Growth Factor Binding
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