SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
WRN-LETM2-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
WRN-LETM2-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
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. [provided by RefSeq, Aug 2017]
Gene Symbol : WRN
Gene Name : Werner syndrome RecQ like helicase
Chromosome : CHR 8: 310,332,61-311,737,60
Locus : 8p12
Gene Symbol : LETM2
Gene Name : Leucine zipper and EF-hand containing transmembrane protein 2
Chromosome : CHR 8: 383,825,04-384,095,26
Locus : 8p11.23
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