PHF6 anticorps (AA 125-175)

N° du produit ABIN7448999

L’anticorps Lapin Polyclonal anti-PHF6 a été validé pour IHC et IF (p). Il convient pour détecter PHF6 dans des échantillons de Humain et Souris.

Aperçu rapide pour PHF6 anticorps (AA 125-175) (ABIN7448999)

Antigène: PHF6 (PHD Finger Protein 6 (PHF6))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PHF6 est non-conjugé

Application: Immunohistochemistry (IHC), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-PHF6 anticorps

Épitope: AA 125-175

Fonction: Rabbit anti-PHF6 IHC Antibody, Affinity Purified

Homologie: Bovine,Dog,Horse,Rabbit,Pig,Panda,Orangutan,Monkey,Gorilla,Chimpanzee,Thirteen-lined ground squirrel,Small-eared galago,Northern white-cheeked gibbon,Little brown bat,Ferret,Crab-eating macaque,White-tufted-ear marmoset,Naked mole rat,Chinese hamster

Purification: Affinity Purified

Immunogène: Between AA 125 and 175

Isotype: IgG

Information d'application

Indications d'application:

IHC-IF: 1:50 - 1:500

IHC: 1:100 - 1:500

Restrictions: For Research Use only

Stockage

Concentration: 250 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

Agent conservateur: Sodium azide

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

Stock: 4 °C

Date de péremption: 12 months

Détails sur PHF6

Antigène: PHF6 (PHD Finger Protein 6 (PHF6))

Autre désignation: PHF6

Sujet: Background: PHF6 a member of the PHD (plant homeodomain)-like zinc-finger family of proteins and is suggested to function as an important transcription factor. PHF6 is ubiquitously expressed and localizes to the cell nucleus with prominent expression in the nucleolus. Expression in the nucleolus indicates an importance to ribosome biogenesis. Mutations in PHF6 are the cause of Borgeson-Forssman-Lehman syndrome (BFLS), an X-linked syndrome characterized by mental retardation, hypogonadism, hypometabolism, obesity, gynecomastia, and several forms of facial anomalies.

ID gène: 84295

NCBI Accession: NP_115834

UniProt: Q8IWS0