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WWOX-C15ORF41 Fusion FISH Probe

The WWOX-C15ORF41 Fusion FISH Probe is used to confirm a fusion of the WWOX and C15ORF41 genes. The fusion of the WWOX and C15ORF41 genes has been associated with Glioblastoma Multiforme. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
WWOX-C15ORF41-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
WWOX-C15ORF41-20-RERE 20 (40 μL) 200 μL
WWOX-C15ORF41-20-REOR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-REGO 20 (40 μL) 200 μL
WWOX-C15ORF41-20-REGR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-REAQ 20 (40 μL) 200 μL
WWOX-C15ORF41-20-ORRE 20 (40 μL) 200 μL
WWOX-C15ORF41-20-OROR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-ORGO 20 (40 μL) 200 μL
WWOX-C15ORF41-20-ORAQ 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GORE 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GOOR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GOGO 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GOGR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GOAQ 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GRRE 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GROR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GRGO 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GRGR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-GRAQ 20 (40 μL) 200 μL
WWOX-C15ORF41-20-AQRE 20 (40 μL) 200 μL
WWOX-C15ORF41-20-AQOR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-AQGO 20 (40 μL) 200 μL
WWOX-C15ORF41-20-AQGR 20 (40 μL) 200 μL
WWOX-C15ORF41-20-AQAQ 20 (40 μL) 200 μL

WWOX Gene Summary

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 Name: WW Domain Containing Oxidoreductase

Chromosome: CHR16: 78133326 -79246564

Locus: 16q23.1-q23.2

C15orf41 Gene Summary

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 Name: Chromosome 15 Open Reading Frame 41

Chromosome: CHR15: 36871811 -37102449

Locus: 15q14

Gene Diseases

The WWOX C15ORF41 Fusion has been associated with the following diseases:

Disease Name
Glioblastoma Multiforme

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.