DCUN1D1-CCDC50 Fusion FISH Probe
The DCUN1D1-CCDC50 Fusion FISH Probe is used to confirm a fusion of the DCUN1D1 and CCDC50 genes. The fusion of the DCUN1D1 and CCDC50 genes has been associated with Breast Invasive Carcinoma. 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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| DCUN1D1-CCDC50-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-RERE | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-REOR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-REGO | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-REGR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-REAQ | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-ORRE | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-OROR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-ORGO | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-ORAQ | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GORE | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GOOR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GOGO | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GOGR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GOAQ | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GRRE | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GROR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GRGO | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GRGR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-GRAQ | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-AQRE | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-AQOR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-AQGO | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-AQGR | 20 (40 μL) | 200 μL |
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| DCUN1D1-CCDC50-20-AQAQ | 20 (40 μL) | 200 μL |
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DCUN1D1 Gene Summary
The Defective In Cullin Neddylation 1 Domain Containing 1 (DCUN1D1) gene is located on chr3 :182660558-182698326 at 3q26.33.
Gene Name: Defective In Cullin Neddylation 1 Domain Containing 1
Chromosome: CHR3: 182660558 -182698326
Locus: 3q26.33
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
Gene Diseases
The DCUN1D1 CCDC50 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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