PHF6 anticorps (AA 315-349)

N° du produit ABIN5647227

Détail du produit anti-PHF6 anticorps

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

Épitope: AA 315-349

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PHF6 est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée (Details): Expected species reactivity: Bovine

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 315-349 from the human protein was used as the immunogen for the PHF6 antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: Western blot: 1:1000-2000

Restrictions: For Research Use only

Stockage

Buffer: In 1X PBS, pH 7.4, with 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: -20 °C

Stockage commentaire: Aliquot the PHF6 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Détails sur PHF6

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

Autre désignation: PHF6 / PHD finger protein 6 (PHF6 Produits)

Synonymes: anticorps zgc:55403, anticorps wu:fa22g03, anticorps BFLS, anticorps BORJ, anticorps CENP-31, anticorps 2700007B13Rik, anticorps 4931428F02Rik, anticorps mKIAA1823, anticorps PHD finger protein 6, anticorps PHD finger protein 6 L homeolog, anticorps phf6, anticorps phf6.L, anticorps PHF6, anticorps Phf6

Sujet: This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes PHD finger protein 6, 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 mental retardation, 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. [RefSeq]

ID gène: 84295

UniProt: Q8IWS0