FOXN1 anticorps (AA 321-420) (AbBy Fluor® 647)

N° du produit ABIN1397715

Cet anticorps anti-FOXN1 est un anticorps Lapin Polyclonal détectant FOXN1 dans WB, FACS, IF (cc) et IF (p). Adapté pour Humain, Rat et Souris.

Aperçu rapide pour FOXN1 anticorps (AA 321-420) (AbBy Fluor® 647) (ABIN1397715)

Antigène: FOXN1 (Forkhead Box N1 (FOXN1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXN1 est conjugé à/à la AbBy Fluor® 647

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-FOXN1 anticorps (AbBy Fluor® 647)

Épitope: AA 321-420

Réactivité croisée: Humain, Souris, Rat

Homologie: Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FOXN1

Isotype: IgG

Information d'application

Indications d'application: FCM 1:20-100
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur FOXN1

Antigène: FOXN1 (Forkhead Box N1 (FOXN1))

Autre désignation: FOXN1

Sujet:

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].

ID gène: 8456

UniProt: O15353