NSUN5 antibody (AA 277-466)

Catalog No. ABIN7268955

Product Details anti-NSUN5 Antibody

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

Binding Specificity: AA 277-466

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NSUN5 antibody is un-conjugated

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

Purpose: NSUN5 Rabbit pAb

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

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Application Details

Application Notes: WB,1:200 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

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

Storage: -20 °C

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

Target Details for NSUN5

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

Alternative Name: NSUN5 (NSUN5 Products)

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

Background: 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

Molecular Weight: 36kDa/42kDa/46kDa/50kDa/51kDa

Gene ID: 55695

UniProt: Q96P11