NSUN3 Antikörper (AA 12-310) (PE)

Produktnummer ABIN8016119

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch NSUN3 in FACS. Es zeigt Reaktivität gegenüber Proben von Human und Affe.

Kurzübersicht für NSUN3 Antikörper (AA 12-310) (PE) (ABIN8016119)

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

Reaktivität: Human, Affe

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NSUN3 Antikörper ist konjugiert mit PE

Applikation: Flow Cytometry (FACS)

Produktdetails anti-NSUN3 Antikörper (PE)

Bindungsspezifität: AA 12-310

Verwendungszweck: Anti-NSUN3 Antibody PE Conjugated

Kreuzreaktivität (Details): No cross-reactivity with other proteins.

Aufreinigung: Immunogen affinity purified.

Immunogen: E.coli-derived human NSUN3 recombinant protein (Position: K12-E310).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Details zu NSUN3

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

Andere Bezeichnung: NSUN3

Hintergrund:

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

Gene Full Name: NOP2/Sun RNA methyltransferase 3

Gen-ID: 63899

UniProt: Q9H649