CHCHD6-UBA5 Fusion FISH Probe
The CHCHD6-UBA5 Fusion FISH Probe is used to confirm a fusion of the CHCHD6 and UBA5 genes. The fusion of the CHCHD6 and UBA5 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CHCHD6-UBA5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-RERE | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-REOR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-REGO | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-REGR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-REAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-ORRE | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-OROR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-ORGO | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-ORAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GORE | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GOOR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GOGO | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GOGR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GOAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GRRE | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GROR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GRGO | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GRGR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-GRAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-AQRE | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-AQOR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-AQGO | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-AQGR | 20 (40 μL) | 200 μL |
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| CHCHD6-UBA5-20-AQAQ | 20 (40 μL) | 200 μL |
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UBA5 Gene Summary
This gene encodes a member of the E1-like ubiquitin-activating enzyme family. This protein activates ubiquitin-fold modifier 1, a ubiquitin-like post-translational modifier protein, via the formation of a high-energy thioester bond. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been identified on chromosome 1. [provided by RefSeq, Feb 2016]
Gene Name: Ubiquitin Like Modifier Activating Enzyme 5
Chromosome: CHR3: 132373289 -132396944
Locus: 3q22.1
CHCHD6 Gene Summary
The Coiled-coil-helix-coiled-coil-helix Domain Containing 6 (CHCHD6) gene is located on chr3 :126423117-126679244 at 3q21.3.
Gene Name: Coiled-coil-helix-coiled-coil-helix Domain Containing 6
Chromosome: CHR3: 126423117 -126679244
Locus: 3q21.3
Gene Diseases
The CHCHD6 UBA5 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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