CHD8 anticorps (AA 10-428)

N° du produit ABIN7869704

Cet anticorps Lapin Polyclonal détecte spécifiquement CHD8 dans WB, IHC (p), ELISA et FACS. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour CHD8 anticorps (AA 10-428) (ABIN7869704)

Antigène: CHD8 (Chromodomain Helicase DNA Binding Protein 8 (CHD8))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CHD8 est non-conjugé

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

Détail du produit anti-CHD8 anticorps

Épitope: AA 10-428

Fonction: CHD8 Antibody / Chromodomain-helicase-DNA-binding protein 8

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (D10-A428) was used as the immunogen for the CHD8 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the CHD8 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

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

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the CHD8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur CHD8

Antigène: CHD8 (Chromodomain Helicase DNA Binding Protein 8 (CHD8))

Autre désignation: CHD8

Sujet: Chromodomain-helicase-DNA-binding protein 8 is an enzyme that in humans is encoded by the CHD8 gene. This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants.

UniProt: Q9HCK8

Pathways: Chromatin Binding