WRN (phospho Ser1141) Polyclonal Antibody - RA36207

WRN (phospho Ser1141) Polyclonal Antibody Sizes: 50μL, 100μL Catalogue Numbers: RA36207-50, RA36207-100 Citations, Manuals and MSDS Available upon request. Background: Werner syndrome RecQ like helicase (WRN) Homo sapiens This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging. [provided by RefSeq, Jul 2008], Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. Storage Instructions: -20°C/1 year Recommended dilutions: Western Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications. Alternative Names: WRN; RECQ3; RECQL2; Werner syndrome ATP-dependent helicase; DNA helicase; RecQ-like type 3; RecQ3; Exonuclease WRN; RecQ protein-like 2 Applications: WB; ELISA Species Cross-Reactivity: Human; Rat; Mouse GeneID (Human): 7486 Protein MW (KDa): 162 SWISS: Q14191 Source: Rabbit Research Use Only