MBNL1-NMNAT3 Fusion FISH Probe
The MBNL1-NMNAT3 Fusion FISH Probe is used to confirm a fusion of the MBNL1 and NMNAT3 genes. The fusion of the MBNL1 and NMNAT3 genes has been associated with Prostate Adenocarcinoma. 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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| MBNL1-NMNAT3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-RERE | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-REOR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-REGO | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-REGR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-REAQ | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-ORRE | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-OROR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-ORGO | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-ORAQ | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GORE | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GOOR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GOGO | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GOGR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GOAQ | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GRRE | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GROR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GRGO | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GRGR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-GRAQ | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-AQRE | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-AQOR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-AQGO | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-AQGR | 20 (40 μL) | 200 μL |
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| MBNL1-NMNAT3-20-AQAQ | 20 (40 μL) | 200 μL |
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MBNL1 Gene Summary
This gene encodes a member of the muscleblind protein family which was initially described in Drosophila melanogaster. The encoded protein is a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Mice lacking this gene exhibited muscle abnormalities and cataracts. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. The different isoforms are thought to have different binding specificities and/or splicing activities. [provided by RefSeq, Sep 2015]
Gene Name: Muscleblind Like Splicing Regulator 1
Chromosome: CHR3: 151985828 -152183568
Locus: 3q25.1-q25.2
NMNAT3 Gene Summary
This gene encodes a member of the nicotinamide/nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide, respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]
Gene Name: Nicotinamide Nucleotide Adenylyltransferase 3
Chromosome: CHR3: 139279022 -139396885
Locus: 3q23
Gene Diseases
The MBNL1 NMNAT3 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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