OPHN1-MAOA Fusion FISH Probe
The OPHN1-MAOA Fusion FISH Probe is used to confirm a fusion of the OPHN1 and MAOA genes. The fusion of the OPHN1 and MAOA 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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| OPHN1-MAOA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-RERE | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-REOR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-REGO | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-REGR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-REAQ | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-ORRE | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-OROR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-ORGO | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-ORAQ | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GORE | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GOOR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GOGO | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GOGR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GOAQ | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GRRE | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GROR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GRGO | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GRGR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-GRAQ | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-AQRE | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-AQOR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-AQGO | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-AQGR | 20 (40 μL) | 200 μL |
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| OPHN1-MAOA-20-AQAQ | 20 (40 μL) | 200 μL |
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MAOA Gene Summary
This gene is one of two neighboring gene family members that encode mitochondrial enzymes which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2012]
Gene Name: Monoamine Oxidase A
Chromosome: CHRX: 43515408 -43606068
Locus: Xp11.3
OPHN1 Gene Summary
This gene encodes a Rho-GTPase-activating protein that promotes GTP hydrolysis of Rho subfamily members. Rho proteins are important mediators of intracellular signal transduction, which affects cell migration and cell morphogenesis. Mutations in this gene are responsible for OPHN1-related X-linked cognitive disability with cerebellar hypoplasia and distinctive facial dysmorhphism. [provided by RefSeq, Jul 2008]
Gene Name: Oligophrenin 1
Chromosome: CHRX: 67262185 -67653299
Locus: Xq12
Gene Diseases
The OPHN1 MAOA 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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