FAM193A-NMU Fusion FISH Probe
The FAM193A-NMU Fusion FISH Probe is used to confirm a fusion of the FAM193A and NMU genes. The fusion of the FAM193A and NMU genes has been associated with Uveal 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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| FAM193A-NMU-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-RERE | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-REOR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-REGO | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-REGR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-OROR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GORE | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GROR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM193A-NMU-20-AQAQ | 20 (40 μL) | 200 μL |
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FAM193A Gene Summary
The Family With Sequence Similarity 193 Member A (FAM193A) gene is located on chr4 :2627158-2734302 at 4p16.3.
Gene Name: Family With Sequence Similarity 193 Member A
Chromosome: CHR4: 2627158 -2734302
Locus: 4p16.3
NMU Gene Summary
This gene encodes a member of the neuromedin family of neuropeptides. The encoded protein is a precursor that is proteolytically processed to generate a biologically active neuropeptide that plays a role in pain, stress, immune-mediated inflammatory diseases and feeding regulation. Increased expression of this gene was observed in renal, pancreatic and lung cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. Some of these isoforms may undergo similar processing to generate the mature peptide. [provided by RefSeq, Jul 2015]
Gene Name: Neuromedin U
Chromosome: CHR4: 56461397 -56502465
Locus: 4q12
Gene Diseases
The FAM193A NMU Fusion has been associated with the following diseases:
| Disease Name |
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| Uveal Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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