CHCHD6-MYO1A Fusion FISH Probe
The CHCHD6-MYO1A Fusion FISH Probe is used to confirm a fusion of the CHCHD6 and MYO1A genes. The fusion of the CHCHD6 and MYO1A genes has been associated with Skin Cutaneous 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CHCHD6-MYO1A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-RERE | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-REOR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-REGO | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-REGR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-REAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-ORRE | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-OROR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-ORGO | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-ORAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GORE | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GOOR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GOGO | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GOGR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GOAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GRRE | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GROR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GRGO | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GRGR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-GRAQ | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-AQRE | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-AQOR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-AQGO | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-AQGR | 20 (40 μL) | 200 μL |
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| CHCHD6-MYO1A-20-AQAQ | 20 (40 μL) | 200 μL |
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MYO1A Gene Summary
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011]
Gene Name: Myosin IA
Chromosome: CHR12: 57422300 -57443893
Locus: 12q13.3
CHCHD6 Gene Summary
The Coiled-coil-helix-coiled-coil-helix Domain Containing 6 (CHCHD6) gene is located on chr3 :126423117-126679244 at 3q21.3.
Gene Name: Coiled-coil-helix-coiled-coil-helix Domain Containing 6
Chromosome: CHR3: 126423117 -126679244
Locus: 3q21.3
Gene Diseases
The CHCHD6 MYO1A Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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