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WB analysis of human brain (cerebellum) lysate using GTX89199 FOXP2 antibody, Internal. Dilution : 0.3microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain (cerebellum) lysate using GTX89199 FOXP2 antibody, Internal. Dilution : 0.3microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain (cerebellum) lysate using GTX89199 FOXP2 antibody, Internal. Dilution : 0.3microg/ml Loading : 35microg protein in RIPA buffer

FOXP2 antibody, Internal

GTX89199
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Rat
TargetFOXP2
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Overview

  • Supplier
    GeneTex
  • Product Name
    FOXP2 antibody, Internal
  • Delivery Days Customer
    7
  • Antibody Specificity
    This antibody is expected to recognize isoform I (NP_055306.1), isoform II (NP_683696.2), isoform IV (NP_683698.2) and isoform V (NP_001166237.1).
  • Application Supplier Note
    WB: 0.3-1microg/ml. IHC-P: 2-4microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID93986
  • Target name
    FOXP2
  • Target description
    forkhead box P2
  • Target synonyms
    CAG repeat protein 44; CAGH44; forkhead box protein P2; forkhead/winged-helix transcription factor; SPCH1; TNRC10; trinucleotide repeat containing 10; trinucleotide repeat-containing gene 10 protein
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO15409
  • Protein Name
    Forkhead box protein P2
  • Scientific Description
    This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
  • Reactivity
    Human, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203