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FOXN1 polyclonal antibody

  • Catalog # : PAB6466
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of FOXN1.
  • Immunogen:
  • A synthetic peptide corresponding to human FOXN1.
  • Sequence:
  • C-SVYLSPSSKPVALA
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 68.9
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:32000)
    Immunohistochemistry (20-30 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • 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.
  • Publication Reference
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • FOXN1 polyclonal antibody (Cat # PAB6466) staining (20 ug/mL) of paraffin embedded human thymus medulla. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.
  • ELISA
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 8456
  • Gene Name:
  • FOXN1
  • Gene Alias:
  • FKHL20,RONU,WHN
  • Gene Description:
  • forkhead box N1
  • Gene Summary:
  • Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq
  • Other Designations:
  • Rowett nude,winged helix nude,winged-helix nude
  • Related Disease
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