PHF6 antibody (AA 37-309)

Catalog No. ABIN7874395

The Rabbit Polyclonal anti-PHF6 antibody (ABIN7874395) specifically detects PHF6 in WB, ELISA, IF, IHC (p) and FACS. The antibody is reactive with Human, Mouse, Rat and Monkey samples.

Quick Overview for PHF6 antibody (AA 37-309) (ABIN7874395)

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

Reactivity: Human, Mouse, Rat, Monkey

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PHF6 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Product Details anti-PHF6 Antibody

Binding Specificity: AA 37-309

Purpose: PHF6 Antibody / PHD finger protein 6

Purification: Antigen affinity chromatography

Immunogen: An E.coli-derived human recombinant protein (amino acids Q37-D309) was used as the immunogen for the PHF6 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the PHF6 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the PHF6 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for PHF6

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

Alternative Name: PHF6

Background: PHD finger protein 6 is a protein that in humans is encoded by the PHF6 gene. This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms.

UniProt: Q8IWS0