NSUN3 antibody (AA 12-310)

Catalog No. ABIN7870286

This Rabbit Polyclonal antibody specifically detects NSUN3 in WB, ELISA and FACS. It exhibits reactivity toward Human and Monkey.

Quick Overview for NSUN3 antibody (AA 12-310) (ABIN7870286)

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

Reactivity: Human, Monkey

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NSUN3 antibody is un-conjugated

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

Product Details anti-NSUN3 Antibody

Binding Specificity: AA 12-310

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

Purification: Antigen affinity purified

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

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the NSUN3 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 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.

Target Details for NSUN3

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

Alternative Name: NSUN3

Background: 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