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Last updated: 2019/12/8

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FOXP2 monoclonal antibody, clone 5C11A8 

  • Catalog # : MAB17707
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against recombinant human FOXP2.
  • Immunogen:
  • Recombinant protein corresponding to human FOXP2 from E. coli.
  • Host:
  • Mouse
  • Theoretical MW (kDa):
  • 85
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Isotype:
  • IgG1
  • Recommend Usage:
  • ELISA (1:10000)
    Flow Cytometry
    Immunocytochemistry
    Immunohistochemistry
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In ascites (0.03% sodium azide).
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Enzyme-linked Immunoabsorbent Assay
  • ELISA analysis of FOXP2 monoclonal antibody, clone 5C11A8.
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Enzyme-linked Immunoabsorbent Assay
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  • Gene Information
  • Gene Name:
  • FOXP2
  • Gene Alias:
  • CAGH44,DKFZp686H1726,SPCH1,TNRC10
  • Gene Description:
  • forkhead box P2
  • Gene Summary:
  • This gene encodes an evolutionarily conserved transcription factor expressed in fetal and adult brain. This transcription factor is a member of the forkhead/winged-helix (FOX) family of transcription factors, and contains a FOX DNA-binding domain and a large polyglutamine tract. Members of the FOX family of transcription factors are regulators of embryogenesis. The product of this gene is thought to be required for proper development of speech and language regions of the brain during embryogenesis. Although a point mutation in this gene has been associated with the KE pedigree segregating developmental verbal dyspraxia, no association between mutations in this gene and another speech disorder, autism, has been found. Multiple alternative transcripts encoding different isoforms have been identified. [provided by RefSeq
  • Other Designations:
  • CAG repeat protein 44,OTTHUMP00000067772,forkhead/winged-helix transcription factor,speech and language disorder 1,trinucleotide repeat containing 10
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