ATN1-ENO2 Fusion FISH Probe
The ATN1-ENO2 Fusion FISH Probe is used to confirm a fusion of the ATN1 and ENO2 genes. The fusion of the ATN1 and ENO2 genes has been associated with Liver Hepatocellular 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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| ATN1-ENO2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-RERE | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-REOR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-REGO | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-REGR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-REAQ | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-ORRE | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-OROR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-ORGO | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GORE | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GOOR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GOGO | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GOGR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GRRE | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GROR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GRGO | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GRGR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-AQRE | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-AQOR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-AQGO | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-AQGR | 20 (40 μL) | 200 μL |
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| ATN1-ENO2-20-AQAQ | 20 (40 μL) | 200 μL |
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ATN1 Gene Summary
Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein. [provided by RefSeq, Jul 2016]
Gene Name: Atrophin 1
Chromosome: CHR12: 7033625 -7051484
Locus: 12p13.31
ENO2 Gene Summary
This gene encodes one of the three enolase isoenzymes found in mammals. This isoenzyme, a homodimer, is found in mature neurons and cells of neuronal origin. A switch from alpha enolase to gamma enolase occurs in neural tissue during development in rats and primates. [provided by RefSeq, Jul 2008]
Gene Name: Enolase 2
Chromosome: CHR12: 7023613 -7032859
Locus: 12p13.31
Gene Diseases
The ATN1 ENO2 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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