CCDC75-DYM Fusion FISH Probe
The CCDC75-DYM Fusion FISH Probe is used to confirm a fusion of the CCDC75 and DYM genes. The fusion of the CCDC75 and DYM 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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| CCDC75-DYM-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-RERE | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-REOR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-REGO | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-REGR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-REAQ | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-ORRE | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-OROR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-ORGO | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-ORAQ | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GORE | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GOOR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GOGO | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GOGR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GOAQ | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GRRE | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GROR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GRGO | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GRGR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-GRAQ | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-AQRE | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-AQOR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-AQGO | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-AQGR | 20 (40 μL) | 200 μL |
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| CCDC75-DYM-20-AQAQ | 20 (40 μL) | 200 μL |
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DYM Gene Summary
This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]
Gene Name: Dymeclin
Chromosome: CHR18: 46570171 -46987079
Locus: 18q21.1
Gene Diseases
The CCDC75 DYM 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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