ZNF429-C2CD3 Fusion FISH Probe
The ZNF429-C2CD3 Fusion FISH Probe is used to confirm a fusion of the ZNF429 and C2CD3 genes. The fusion of the ZNF429 and C2CD3 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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| ZNF429-C2CD3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-RERE | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-REOR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-REGO | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-REGR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-REAQ | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-ORRE | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-OROR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-ORGO | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-ORAQ | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GORE | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GOOR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GOGO | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GOGR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GOAQ | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GRRE | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GROR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GRGO | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GRGR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-GRAQ | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-AQRE | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-AQOR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-AQGO | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-AQGR | 20 (40 μL) | 200 μL |
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| ZNF429-C2CD3-20-AQAQ | 20 (40 μL) | 200 μL |
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C2CD3 Gene Summary
This gene encodes a protein that functions as a regulator of centriole elongation. Studies of the orthologous mouse protein show that it promotes centriolar distal appendage assembly and is also required for the recruitment of other ciliogenic proteins, including intraflagellar transport proteins. Mutations in this gene cause orofaciodigital syndrome XIV (OFD14), a ciliopathy resulting in malformations of the oral cavity, face and digits. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Gene Name: C2 Calcium Dependent Domain Containing 3
Chromosome: CHR11: 73745479 -73882064
Locus: 11q13.4
ZNF429 Gene Summary
The Zinc Finger Protein 429 (ZNF429) gene is located on chr19 :21688436-21721079 at 19p12.
Gene Name: Zinc Finger Protein 429
Chromosome: CHR19: 21688436 -21721079
Locus: 19p12
Gene Diseases
The ZNF429 C2CD3 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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