NSUN3 anticorps (AA 12-310)

N° du produit ABIN7870286

Cet anticorps Lapin Polyclonal détecte spécifiquement NSUN3 dans WB, ELISA et FACS. Il présente une réactivité avec des échantillons de Humain et Singe.

Aperçu rapide pour NSUN3 anticorps (AA 12-310) (ABIN7870286)

Antigène: NSUN3 (NOP2/Sun Domain Family, Member 3 (NSUN3))

Reactivité: Humain, Singe

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSUN3 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-NSUN3 anticorps

Épitope: AA 12-310

Fonction: NSUN3 Antibody / NOL1/NOP2/Sun domain family member 3 / MST077

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (K12-E310) was used as the immunogen for the NSUN3 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the NSUN3 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 NSUN3 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 NSUN3

Antigène: NSUN3 (NOP2/Sun Domain Family, Member 3 (NSUN3))

Autre désignation: NSUN3

Sujet: NSUN3 (NOL1/NOP2/Sun domain family, member 3), also known as MST077, is a 340 amino acid protein that belongs to the methyltransferase superfamily and is thought to function as an S-adenosyl-L-methionine-dependent methyltransferase. The gene encoding NSUN3 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3

UniProt: Q9H649