ITN0078
ITN0078
ITN0078
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$424.00
Price in reward points: 424
- Catalog: ITN0078
- Gene/Protein: FOXN1 RONU WHN
- Product Description: Immunotag™ FOXN1 Polyclonal Antibody
Available Options
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Description
Immunotag™ FOXN1 Polyclonal Antibody
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Specifications
Antibody Specification Datasheet 
IMPORTANT NOTE This product is custom manufactured with a lead time of 3-4 weeks. Once in production, this item cannot be cancelled from an order and is not eligible for return. Target Protein FOXN1 Clonality Polyclonal Storage/Stability -20°C/1 year Application WB,ELISA Recommended Dilution WB 1:500-2000 ELISA 1:5000-20000 Concentration 1 mg/ml Reactive Species Human Host Species Rabbit Immunogen Synthesized peptide derived from human protein . at AA range: 340-420 Specificity FOXN1 Polyclonal Antibody detects endogenous levels of protein. Purification The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen Form Liquid in PBS containing 50% glycerol, and 0.02% sodium azide. Gene Name FOXN1 RONU WHN Accession No. O15353 Q61575 Description forkhead box N1(FOXN1) Homo sapiens Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008], Protein Expression Thymus, Subcellular Localization nucleus, Protein Function disease:Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy [MIM:601705].,function:Transcriptional regulator involved in development.,online information:FOXN1 mutation db,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in thymus., Usage For Research Use Only! Not for diagnostic or therapeutic procedures. - Reviews
| Antibody Specification | |
| Datasheet | |
| IMPORTANT NOTE | This product is custom manufactured with a lead time of 3-4 weeks. Once in production, this item cannot be cancelled from an order and is not eligible for return. |
| Target Protein | FOXN1 |
| Clonality | Polyclonal |
| Storage/Stability | -20°C/1 year |
| Application | WB,ELISA |
| Recommended Dilution | WB 1:500-2000 ELISA 1:5000-20000 |
| Concentration | 1 mg/ml |
| Reactive Species | Human |
| Host Species | Rabbit |
| Immunogen | Synthesized peptide derived from human protein . at AA range: 340-420 |
| Specificity | FOXN1 Polyclonal Antibody detects endogenous levels of protein. |
| Purification | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen |
| Form | Liquid in PBS containing 50% glycerol, and 0.02% sodium azide. |
| Gene Name | FOXN1 RONU WHN |
| Accession No. | O15353 Q61575 |
| Description | forkhead box N1(FOXN1) Homo sapiens Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008], |
| Protein Expression | Thymus, |
| Subcellular Localization | nucleus, |
| Protein Function | disease:Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy [MIM:601705].,function:Transcriptional regulator involved in development.,online information:FOXN1 mutation db,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:Expressed in thymus., |
| Usage | For Research Use Only! Not for diagnostic or therapeutic procedures. |