Synthetic peptide, conjugated to KLH, corresponding to residues in Human FOXN1.
Human Uterus tissue; Raji whole cell lysate.
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.01% Thimerosal (merthiolate) Constituents: 10% Glycerol, 89% PBS
Concentration information loading...
Protein A 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.
Use a concentration of 10 µg/ml.
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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-FOXN1 antibody (ab113235)
ab113235 at 10ug/ml staining FOXN1 in Formalin-fixed, Paraffin-embedded Human Uterus tissue by Immunohistochemistry.
Western blot - Anti-FOXN1 antibody (ab113235)
Anti-FOXN1 antibody (ab113235) at 1/1000 dilution + Raji whole cell lysate at 30 µg
Predicted band size: 69 kDa 7.5% SDS PAGE.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"