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FGFR3 Protein (Soluble)

FGFR3 Origine: Humain Hôte: Cellules d'insectes Recombinant > 95 % by SDS-PAGE
N° du produit ABIN7539328
  • Antigène Voir toutes FGFR3 Protéines
    FGFR3 (Fibroblast Growth Factor Receptor 3 (FGFR3))
    Type de proteíne
    Recombinant
    Attributs du protein
    Soluble
    Origine
    • 20
    • 4
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 7
    • 7
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    Cellules d'insectes
    Fonction
    FGFR-3(IIIa), soluble
    Séquence
    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
    Specificité
    Chromosomal location:4q16.3
    Attributs du produit
    Length (aa):290
    Pureté
    > 95 % by SDS-PAGE
    Top Product
    Discover our top product FGFR3 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
  • Antigène
    FGFR3 (Fibroblast Growth Factor Receptor 3 (FGFR3))
    Autre désignation
    FGFR-3 (FGFR3 Produits)
    Synonymes
    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
    Sujet
    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.
    Poids moléculaire
    31.7 kDa
    ID gène
    2261
    NCBI Accession
    NM_022965, NP_075254
    UniProt
    P22607-3
    Pathways
    Signalisation RTK, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, Stem Cell Maintenance, Growth Factor Binding
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