Recombinant Human WRN Protein, 517-1093, N-GST tagged

Cat.No. : WRN-12H
Product Overview : Recombinant human WRN (Werner syndrome ATP-dependent helicase), encompassing amino acids 517-1093. This construct contains an N-terminal GST-tag followed by a Thrombin cleavage site. The recombinant protein was affinity purified.
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Species : Human
Source : Sf9 Cells
Tag : GST
Protein Length : 517-1093
Description : This gene encodes a member of the RecQ subfamily of DNA helicase proteins. The encoded nuclear protein is important in the maintenance of genome stability and plays a role in DNA repair, replication, transcription and telomere maintenance. This protein contains a N-terminal 3' to 5' exonuclease domain, an ATP-dependent helicase domain and RQC (RecQ helicase conserved region) domain in its central region, and a C-terminal HRDC (helicase RNase D C-terminal) domain and nuclear localization signal. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by accelerated aging and an elevated risk for certain cancers.
Form : Aqueous buffer solution
Molecular Mass : 92 kDa
Purity : 0.9
Notes : Avoid freeze/thaw cycles
Usage : Thaw on ice and gently mix prior to use. DO NOT VORTEX. Perform a quick spin before opening. Aliquot into small volumes and flash freeze for long term storage. Avoid multiple freeze/thaw cycles.
Storage : At least 6 months at -80 centigrade.
Storage Buffer : 40 mM Tris-HCl, pH 8.0, 200 mM NaCl, 2.2 mM KCl, 0.05% Tween-20, 10 mM glutathione, 1 mM TCEP, and 20% glycerol
Shipping : At -80 centigrade
Gene Name WRN WRN RecQ like helicase [ Homo sapiens (human) ]
Official Symbol WRN
Synonyms WRN; WRN RecQ like helicase; RECQ3; RECQL2; RECQL3; bifunctional 3'-5' exonuclease/ATP-dependent helicase WRN; DNA helicase, RecQ-like type 3; Werner syndrome ATP-dependent helicase; Werner syndrome RecQ like helicase; Werner syndrome protein; Werner syndrome, RecQ helicase-like; exonuclease WRN; recQ protein-like 2; EC 3.6.4.12
Gene ID 7486
mRNA Refseq NM_000553
Protein Refseq NP_000544
MIM 604611
UniProt ID Q14191

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