PHF6 antibody (AA 125-175)

Catalog No. ABIN7448999

The Rabbit Polyclonal anti-PHF6 antibody has been validated for IHC and IF (p). It is suitable to detect PHF6 in samples from Human and Mouse.

Quick Overview for PHF6 antibody (AA 125-175) (ABIN7448999)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PHF6 antibody is un-conjugated

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

Product Details anti-PHF6 Antibody

Binding Specificity: AA 125-175

Purpose: Rabbit anti-PHF6 IHC Antibody, Affinity Purified

Predicted Reactivity: 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

Immunogen: Between AA 125 and 175

Isotype: IgG

Application Details

Application Notes:

IHC-IF: 1:50 - 1:500

IHC: 1:100 - 1:500

Restrictions: For Research Use only

Handling

Concentration: 250 μg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C

Expiry Date: 12 months

Target Details for PHF6

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

Alternative Name: PHF6

Background: 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.

Gene ID: 84295

NCBI Accession: NP_115834

UniProt: Q8IWS0