ANKRD11-CPNE7 Fusion FISH Probe
The ANKRD11-CPNE7 Fusion FISH Probe is used to confirm a fusion of the ANKRD11 and CPNE7 genes. The fusion of the ANKRD11 and CPNE7 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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| ANKRD11-CPNE7-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-RERE | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-REOR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-REGO | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-REGR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-REAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-ORRE | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-OROR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-ORGO | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-ORAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GORE | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GOOR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GOGO | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GOGR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GOAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GRRE | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GROR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GRGO | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GRGR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-GRAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-AQRE | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-AQOR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-AQGO | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-AQGR | 20 (40 μL) | 200 μL |
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| ANKRD11-CPNE7-20-AQAQ | 20 (40 μL) | 200 μL |
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CPNE7 Gene Summary
This gene encodes a member of the copine family, which is composed of calcium-dependent membrane-binding proteins. The gene product contains two N-terminal C2 domains and one von Willebrand factor A domain. The encoded protein may be involved in membrane trafficking. Two alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
Gene Name: Copine 7
Chromosome: CHR16: 89642175 -89663654
Locus: 16q24.3
ANKRD11 Gene Summary
This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012]
Gene Name: Ankyrin Repeat Domain 11
Chromosome: CHR16: 89334034 -89556969
Locus: 16q24.3
Gene Diseases
The ANKRD11 CPNE7 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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