|Other Names||Forkhead box protein N1, Winged-helix transcription factor nude, FOXN1, RONU, WHN|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.|
|Precautions||This product is for research use only. Not for use in diagnostic or therapeutic procedures.|
|Function||Transcriptional regulator which regulates the development, differentiation, and function of thymic epithelial cells (TECs) both in the prenatal and postnatal thymus. Acts as a master regulator of the TECs lineage development and is required from the onset of differentiation in progenitor TECs in the developing fetus to the final differentiation steps through which TECs mature to acquire their full functionality. Regulates, either directly or indirectly the expression of a variety of genes that mediate diverse aspects of thymus development and function, including MHC Class II, DLL4, CCL25, CTSL, CD40 and PAX1. Regulates the differentiation of the immature TECs into functional cortical TECs (cTECs) and medullary TECs (mTECs). Essential for maintenance of mTECs population in the postnatal thymus. Involved in the morphogenesis and maintenance of the three-dimensional thymic microstructure which is necessary for a fully functional thymus. Plays an important role in the maintenance of hematopoiesis and particularly T lineage progenitors within the bone marrow niche with age. Essential for the vascularization of the thymus anlage. Promotes the terminal differentiation of epithelial cells in the epidermis and hair follicles, partly by negatively regulating the activity of protein kinase C (By similarity). Plays a crucial role in the early prenatal stages of T cell ontogeny (PubMed:21507891).|
|Tissue Location||Expressed in thymus.|
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Mutations in the winged-helix transcription factor gene atthe nude locus in mice and rats produce the pleiotropic phenotypeof hairlessness and athymia, resulting in a severely compromisedimmune system. This gene is orthologous to the mouse and rat genesand encodes a similar DNA-binding transcription factor that isthought to regulate keratin gene expression. A mutation in thisgene has been correlated with T-cell immunodeficiency, the skindisorder congenital alopecia, and nail dystrophy. Alternativesplicing in the 5' UTR of this gene has been observed. [provided byRefSeq].
Jugessur, A., et al. PLoS ONE 5 (7), E11493 (2010) :Mandinova, A., et al. J. Clin. Invest. 119(10):3127-3137(2009)Pignata, C., et al. Adv. Exp. Med. Biol. 665, 195-206 (2009) :Weiner, L., et al. Cell 130(5):932-942(2007)Nonaka, D., et al. Am. J. Surg. Pathol. 31(7):1038-1044(2007)
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