| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| WWOX-C15orf41-20-RERE | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-REOR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-REGO | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-REGR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-REAQ | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-ORRE | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-OROR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-ORGO | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-ORGR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-ORAQ | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GORE | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GOOR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GOGO | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GOGR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GOAQ | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GRRE | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GROR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GRGO | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GRGR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-GRAQ | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-AQRE | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-AQOR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-AQGO | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-AQGR | 20 (40 μL) | 200 μL |
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| WWOX-C15orf41-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
Gene Symbol : WWOX
Gene Name : WW domain containing oxidoreductase
Chromosome : CHR 16: 780,994,12-792,126,66
Locus : 16q23.1-q23.2
This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]
Gene Symbol : C15ORF41
Gene Name : Chromosome 15 open reading frame 41
Chromosome : CHR 15: 365,796,02-368,102,59
Locus : 15q14
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