NSUN5 anticorps (AA 277-466)

N° du produit ABIN7268955

Détail du produit anti-NSUN5 anticorps

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

Épitope: AA 277-466

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSUN5 est non-conjugé

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

Fonction: NSUN5 Rabbit pAb

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

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: WB,1:200 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

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

Détails sur NSUN5

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

Autre désignation: NSUN5 (NSUN5 Produits)

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

Sujet: 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

Poids moléculaire: 36kDa/42kDa/46kDa/50kDa/51kDa

ID gène: 55695

UniProt: Q96P11