MYO6-NEGR1 Fusion FISH Probe
The MYO6-NEGR1 Fusion FISH Probe is used to confirm a fusion of the MYO6 and NEGR1 genes. The fusion of the MYO6 and NEGR1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| MYO6-NEGR1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-RERE | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-REOR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-REGO | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-REGR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-REAQ | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-ORRE | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-OROR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-ORGO | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GORE | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GOOR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GOGO | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GOGR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GRRE | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GROR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GRGO | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GRGR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-AQRE | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-AQOR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-AQGO | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-AQGR | 20 (40 μL) | 200 μL |
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| MYO6-NEGR1-20-AQAQ | 20 (40 μL) | 200 μL |
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MYO6 Gene Summary
This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]
Gene Name: Myosin VI
Chromosome: CHR6: 76458908 -76629254
Locus: 6q14.1
NEGR1 Gene Summary
The Neuronal Growth Regulator 1 (NEGR1) gene is located on chr1 :71868624-72748277 at 1p31.1.
Gene Name: Neuronal Growth Regulator 1
Chromosome: CHR1: 71868624 -72748277
Locus: 1p31.1
Gene Diseases
The MYO6 NEGR1 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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