NOL9-ESPN Fusion FISH Probe
The NOL9-ESPN Fusion FISH Probe is used to confirm a fusion of the NOL9 and ESPN genes. The fusion of the NOL9 and ESPN genes has been associated with Uterine Corpus Endometrial 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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| NOL9-ESPN-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-RERE | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-REOR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-REGO | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-REGR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-REAQ | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-ORRE | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-OROR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-ORGO | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-ORAQ | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GORE | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GOOR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GOGO | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GOGR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GOAQ | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GRRE | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GROR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GRGO | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GRGR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-GRAQ | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-AQRE | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-AQOR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-AQGO | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-AQGR | 20 (40 μL) | 200 μL |
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| NOL9-ESPN-20-AQAQ | 20 (40 μL) | 200 μL |
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NOL9 Gene Summary
The Nucleolar Protein 9 (NOL9) gene is located on chr1 :6581406-6614658 at 1p36.31.
Gene Name: Nucleolar Protein 9
Chromosome: CHR1: 6581406 -6614658
Locus: 1p36.31
ESPN Gene Summary
This gene encodes a multifunctional actin-bundling protein. It plays a major role in regulating the organization, dimensions, dynamics, and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in various mechanosensory and chemosensory cells. Mutations in this gene are associated with autosomal recessive neurosensory deafness, and autosomal dominant sensorineural deafness without vestibular involvement. [provided by RefSeq, Nov 2009]
Gene Name: Espin
Chromosome: CHR1: 6484847 -6521004
Locus: 1p36.31
Gene Diseases
The NOL9 ESPN Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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