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BellBrook
WRN Exonuclease (human) (rec.) (His) (active) (5µg)

Product Details | |
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Synonyms | Werner Syndrome Exonuclease; RecQ Protein-like 2; RECQ3; RECQL2; RECQL3; WRN RecQ-like Exonuclease |
Product Type | Protein |
Properties | |
Source/Host | E. coli |
Sequence |
Human Werner syndrome exonuclease (aa 1-333) has a His-tag. |
Crossreactivity | Human |
Application |
Drug Discovery |
Biological Activity |
The enzyme has been thoroughly validated with the Transcreener dAMP Assay Kit. |
MW | 38.9kDa |
Purity | ≥90% (SDS-PAGE) |
Accession Number | Q14191 |
Formulation | Liquid. In 50 mM Tris-HCl, 150 mM NaCl, 10% Glycerol (pH 8.0). |
Other Product Data |
Click here for Complete Information from the Original Manufacturer Uniprot Q14191: WRN HUMAN |
Shipping and Handling | |
Shipping | DRY ICE |
Short Term Storage | -20°C |
Long Term Storage | -80°C |
Handling Advice | Avoid freeze/thaw cycles. |
Use/Stability | Stable for at least 6 months after receipt when stored at -80°C. |
Documents | |
Product Specification Sheet | |
Datasheet |
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The WRN protein is a unique member of the RecQ family of DNA helicases distinguished by its dual enzymatic activities: a 3′→5′ DNA helicase and a 3′→5′ exonuclease. The exonuclease activity, located in the N-terminal domain, enables WRN to process DNA ends and plays a critical role in multiple DNA metabolic pathways, including DNA repair, replication, recombination and telomere maintenance. By coordinating unwinding and degradation of DNA, WRN ensures proper resolution of DNA intermediates and preservation of genomic stability. Mutations that disrupt WRN function lead to Werner syndrome, a rare premature aging disorder marked by genomic instability and increased cancer predisposition. The WRN exonuclease is therefore a central player in maintaining genome integrity and a key subject of study in aging, DNA repair, and cancer biology.