FCHO2-SLC25A17 Fusion FISH Probe
The FCHO2-SLC25A17 Fusion FISH Probe is used to confirm a fusion of the FCHO2 and SLC25A17 genes. The fusion of the FCHO2 and SLC25A17 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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| FCHO2-SLC25A17-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-RERE | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-REOR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-REGO | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-REGR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-REAQ | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-ORRE | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-OROR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-ORGO | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-ORAQ | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GORE | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GOOR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GOGO | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GOGR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GOAQ | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GRRE | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GROR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GRGO | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GRGR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-GRAQ | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-AQRE | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-AQOR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-AQGO | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-AQGR | 20 (40 μL) | 200 μL |
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| FCHO2-SLC25A17-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC25A17 Gene Summary
This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Gene Name: Solute Carrier Family 25 Member 17
Chromosome: CHR22: 41165638 -41215392
Locus: 22q13.2
FCHO2 Gene Summary
The FCH Domain Only 2 (FCHO2) gene is located on chr5 :72251807-72386349 at 5q13.2.
Gene Name: FCH Domain Only 2
Chromosome: CHR5: 72251807 -72386349
Locus: 5q13.2
Gene Diseases
The FCHO2 SLC25A17 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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