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FOXN1 Antibody (720152) in WB
Western blot analysis was performed on nuclear enriched cell extracts (30 µg lysate) of Raji (Lane 1), A549 (Lane 2) and PC-12 (Lane 3). The blots were probed with Anti- FOXN1 Rabbit Polyclonal Antibody (Product # 720152, 0.5-1 µg/mL) and detected by chemiluminescence using Goat anti-Rabbit IgG (Heavy Chain) Superclonal Secondary Antibody, HRP conjugate (Product # A27036, 0.4 µg/mL, 1:2500 dilution). A 69 kDa band corresponding to FOXN1 was observed across cell lines tested. Known quantity of protein samples were electrophoresed using Nove... View More
Product Details
720152
Applications
Tested Dilution
Publications
Product Specifications
Species Reactivity
Human,
Rat
Host/Isotype
Rabbit
/ IgG
Class
Polyclonal
Type
Antibody
Immunogen
Peptide pair corresponding to Human FOXN1 (aa 377-395; 633-646)
Conjugate
Form
Liquid
Concentration
0.5 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.2, with 0.1% BSA, 30% glycerol
Contains
0.09% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2610353
Product Specific Information
These Polyclonal antibodies are of rabbit origin developed by immunizing animals with proteins or peptides. The polyclonal antibody is purified by affinity purification from the rabbit sera generated after immunizing the rabbits with a specific type of protein or peptide. The purified antibody is tested for its functionality in various relevant research applications. The antibody is developed for Research Use Only and is non-hazardous or non-infectious in nature.
Target Information
FOXN1 is a 648 amino acid protein belonging to the winged helix/forkhead family It contains 1 fork-head DNA-binding domain and is a transcriptional regulator involved in development. FOXN1 is involved in directing lineage choices of multi-potential progenitor epithelial cells and controls important regulating genes of lympho-epithelial interactions. It modulates keratinocyte differentiation in hair follicles and nail apparatus and its defects lead to T-cell immunodeficiency congenital alopecia, nail dystrophy, macroscopic nudity and an inborn dysgenesis of the thymus.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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Bioinformatics
Protein Aliases: Forkhead box protein N1; JTK1; Rowett nude; winged helix nude; winged-helix nude; Winged-helix transcription factor nude
Gene Aliases: FKHL20; FOXN1; Rnu; RONU; WHN
UniProt ID: (Human) O15353
Entrez Gene ID: (Human) 8456, (Rat) 287469
hair follicle development
lymphocyte homeostasis
regulation of transcription from RNA polymerase II promoter
transcription from RNA polymerase II promoter
cell proliferation
epidermis development
regulation of gene expression
keratinocyte differentiation
regulation of T cell differentiation in thymus
nail development
thymus development
epithelial cell proliferation
T cell lineage commitment
defense response
organ morphogenesis
positive regulation of epithelial cell differentiation
T cell homeostasis
blood vessel morphogenesis
positive regulation of hair follicle development
lymphoid lineage cell migration into thymus
thymus epithelium morphogenesis
regulation of positive thymic T cell selection
Performance Guarantee
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
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