Rabbit polyclonal to FOXN1
Synthetic peptide corresponding to a region within amino acids 585 - 648 of Human FOXN1 (NP_003584).
HeLa, MOLT4 cell lysates and Raji whole cell lysates
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol, 1X PBS, pH 7.0
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Immunogen affinity purified
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
1/500 - 1/3000. Predicted molecular weight: 69 kDa.
Transcriptional regulator involved in development.
Expressed in thymus.
Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy (TIDAND) [MIM:601705]. A disorder characterized by the association of congenital alopecia, severe T-cell immunodeficiency, and ridging and pitting of all nails.
Contains 1 fork-head DNA-binding domain.
Information by UniProt
Forkhead box N1 antibody
Forkhead box protein N1 antibody
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"