CCDC50-OSTN Fusion FISH Probe
The CCDC50-OSTN Fusion FISH Probe is used to confirm a fusion of the CCDC50 and OSTN genes. The fusion of the CCDC50 and OSTN 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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| CCDC50-OSTN-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-RERE | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-REOR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-REGO | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-REGR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-REAQ | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-ORRE | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-OROR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-ORGO | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-ORAQ | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GORE | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GOOR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GOGO | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GOGR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GOAQ | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GRRE | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GROR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GRGO | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GRGR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-GRAQ | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-AQRE | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-AQOR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-AQGO | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-AQGR | 20 (40 μL) | 200 μL |
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| CCDC50-OSTN-20-AQAQ | 20 (40 μL) | 200 μL |
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CCDC50 Gene Summary
This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Gene Name: Coiled-coil Domain Containing 50
Chromosome: CHR3: 191046873 -191116459
Locus: 3q28
OSTN Gene Summary
The Osteocrin (OSTN) gene is located on chr3 :190930321-190967910 at 3q28.
Gene Name: Osteocrin
Chromosome: CHR3: 190930321 -190967910
Locus: 3q28
Gene Diseases
The CCDC50 OSTN 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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