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IHC-P analysis of human placenta tissue using GTX55622 FGFR2 antibody. Dilution : 1:100
IHC-P analysis of human placenta tissue using GTX55622 FGFR2 antibody. Dilution : 1:100
IHC-P analysis of human placenta tissue using GTX55622 FGFR2 antibody. Dilution : 1:100

FGFR2 antibody

GTX55622
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetFGFR2
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Overview

  • Supplier
    GeneTex
  • Product Name
    FGFR2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID2263
  • Target name
    FGFR2
  • Target description
    fibroblast growth factor receptor 2
  • Target synonyms
    bacteria-expressed kinase; BBDS; BEK; BEK fibroblast growth factor receptor; BFR-1; CD332; CEK3; CFD1; ECT1; fibroblast growth factor receptor 2; JWS; keratinocyte growth factor receptor; KGFR; K-SAM; protein tyrosine kinase, receptor like 14; TK14; TK25
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP21802
  • Protein Name
    Fibroblast growth factor receptor 2
  • Scientific Description
    The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis. Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203