FOXN1 anticorps (AA 321-420)
Aperçu rapide pour FOXN1 anticorps (AA 321-420) (ABIN1387592)
Antigène
Voir toutes FOXN1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 321-420
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Fonction
- FOXN1 Polyclonal Antibody
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Réactivité croisée
- Humain, Souris, Rat
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Homologie
- Dog,Cow,Pig,Horse,Chicken,Rabbit
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human FOXN1
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Isotype
- IgG
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Indications d'application
- WB(1:300-5000),
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
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Date de péremption
- 12 months
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: "EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay. ..." dans: The Journal of experimental medicine, Vol. 214, Issue 3, pp. 623-637, (2017) (PubMed).
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- FOXN1 (Forkhead Box N1 (FOXN1))
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Autre désignation
- FOXN1
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Sujet
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Synonyms: WHN, RONU, FKHL20, Forkhead box protein N1, Winged-helix transcription factor nude, FOXN1
Background: 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].
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ID gène
- 8456
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UniProt
- O15353
Antigène
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