NSUN5 Polyclonal Antibody

SKU: BT-AP12038

Size:100μL

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.

Research_area:Signal transduction

Target_protein:NSUN5

applications:WB, ELISA

Reactivity:Human, Mouse

Clonality:Polyclonal

Clone ID:

Host:Rabbit

Isotype:IgG

Gene Symbol/ Name:Putative methyltransferase NSUN5

Immunogen:The antiserum was produced against synthesized peptide derived from human AMPK alpha around the phosphorylation site of Thr172. AA range:140-189

Storage:-20°C for 1 year

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration:1 mg/ml

Molecular weight(Da):

UniProt accession:Human: Q96P11; Mouse: Q8K4F6

Synonyms:Putative methyltransferase NSUN5 ;EC 2.1.1.-;NOL1-related protein;NOL1R;NOL1/NOP2/Sun domain family member 5;Williams-Beuren syndrome chromosomal region 20A protein

GeneID:Human: 55695