NSUN5 Antikörper (AA 277-466)

Produktnummer ABIN7268955

Produktdetails anti-NSUN5 Antikörper

Target: NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Bindungsspezifität: AA 277-466

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NSUN5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Verwendungszweck: NSUN5 Rabbit pAb

Sequenz: SCCELAEEDF LAVSPSDPRY HEVHYILLDP SCSGSGMPSR QLEEPGAGTP SPVRLHALAG FQQRALCHAL TFPSLQRLVY STCSLCQEEN EDVVRDALQQ NPGAFRLAPA LPAWPHRGLS TFPGAEHCLR ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA AAGACTPPCT

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 277-466 of human NSUN5 (NP_683759.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:200 - 1:2000,IHC,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Details zu NSUN5

Target: NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Andere Bezeichnung: NSUN5 (NSUN5 Produkte)

Synonyme: RGD1309268 antikoerper, wu:fc49f12 antikoerper, zgc:66176 antikoerper, zgc:77183 antikoerper, 9830109N13Rik antikoerper, AI326939 antikoerper, Nol1r antikoerper, Wbscr20 antikoerper, Wbscr20a antikoerper, NOL1 antikoerper, NOL1R antikoerper, NSUN5A antikoerper, WBSCR20 antikoerper, WBSCR20A antikoerper, p120 antikoerper, NOP2/Sun RNA methyltransferase family member 5 antikoerper, NOP2/Sun domain family, member 5 antikoerper, NOL1/NOP2/Sun domain family, member 5 antikoerper, Nsun5 antikoerper, nsun5 antikoerper, NSUN5 antikoerper

Hintergrund: This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.,NSUN5,NOL1,NOL1R,NSUN5A,WBSCR20,WBSCR20A,p120,p120(NOL1),Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,Endocrine & Metabolism,NSUN5

Molekulargewicht: 36kDa/42kDa/46kDa/50kDa/51kDa

Gen-ID: 55695

UniProt: Q96P11