C15ORF41-RAC2 Fusion FISH Probe
The C15ORF41-RAC2 Fusion FISH Probe is used to confirm a fusion of the C15ORF41 and RAC2 genes. The fusion of the C15ORF41 and RAC2 genes has been associated with Skin Cutaneous Melanoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| C15ORF41-RAC2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-RERE | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-REOR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-REGO | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-REGR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-REAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-ORRE | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-OROR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-ORGO | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-ORAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GORE | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GOOR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GOGO | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GOGR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GOAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GRRE | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GROR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GRGO | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GRGR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-GRAQ | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-AQRE | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-AQOR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-AQGO | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-AQGR | 20 (40 μL) | 200 μL |
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| C15ORF41-RAC2-20-AQAQ | 20 (40 μL) | 200 μL |
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RAC2 Gene Summary
This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013]
Gene Name: Rac Family Small GTPase 2
Chromosome: CHR22: 37621309 -37640305
Locus: 22q13.1
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 C15ORF41 RAC2 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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