Key features and details
- Rabbit polyclonal to FOXN1
- Suitable for: WB, IHC-P
- Reacts with: Human
- Isotype: IgG
Product nameAnti-FOXN1 antibody
See all FOXN1 primary antibodies
DescriptionRabbit polyclonal to FOXN1
Tested applicationsSuitable for: WB, IHC-Pmore details
Species reactivityReacts with: Human
Synthetic peptide, conjugated to KLH, corresponding to residues in Human FOXN1.
- Human Uterus tissue; Raji whole cell lysate.
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Abcam is leading the way with our range of recombinant antibodies, knockout-validated antibodies and knockout cell lines, all of which support improved reproducibility.
We are also planning to innovate the way in which we present recommended applications and species on our product datasheets, so that only applications & species that have been tested in our own labs, our suppliers or by selected trusted collaborators are covered by our Abpromise™ guarantee.
In preparation for this, we have started to update the applications & species that this product is Abpromise guaranteed for.
We are also updating the applications & species that this product has been “predicted to work with,” however this information is not covered by our Abpromise guarantee.
Applications & species from publications and Abreviews that have not been tested in our own labs or in those of our suppliers are not covered by the Abpromise guarantee.
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Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Storage bufferpH: 7.00
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol, 89% PBS
Concentration information loading...
PurityProtein A purified
Our Abpromise guarantee covers the use of ab113235 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/500 - 1/3000. Predicted molecular weight: 69 kDa.|
|IHC-P||Use a concentration of 10 µg/ml.|
FunctionTranscriptional regulator involved in development.
Tissue specificityExpressed in thymus.
Involvement in diseaseDefects 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.
Sequence similaritiesContains 1 fork-head DNA-binding domain.
- Information by UniProt
- FKHL20 antibody
- Forkhead box N1 antibody
- Forkhead box protein N1 antibody
ab113235 has been referenced in 1 publication.
- Lin Z et al. Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia. Am J Hum Genet 91:906-11 (2012). PubMed: 23063621