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Size | List Price | Price | Cart |
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100 ug | $365.00 | Add to Cart |
FOX1N or Forkhead box N1 is involved in T-cell development. 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. Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy. A disorder characterized by the association of congenital alopecia, severe T-cell immunodeficiency, and ridging and pitting of all nails. |
Images
FOX1N (Dilution:20μg/ml) staining of paraffin embedded Human Thymus Medulla. Steamed antigen retrieval with citrate buffer pH 6, AP-staining. Protocol on Data-sheet.