WRN Knockout Cell Line - CD BioSciences

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WRN Knockout Cell Line

WRN Knockout Cell Line

SPL-04008

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1 Unit Online Inquiry
Description
17p deletion
Target Information
Target Name WRN
Gene Abbr. WRN
Gene ID 7486
Full Name WRN RecQ like helicase
Alias RECQ3, RECQL2, RECQL3
Species Human
Genomic Locus chr8:31058479
Introduction 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].
Product Details
Cell Line Model HAP1
Genotype WRN 17bp deletion knockout
Description 17p deletion
Parental Cell Line C631
Handling Specifications
Culture Medium IMDM + 10% FBS
Disclaimer This product is classified under IATA regulations as a GMMO (genetically modified micro-organism) and will ship as UN3245. If applicable, ensure facility meets all requirements per local and country regulations.

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