MYO7A-ZNF512 Fusion FISH Probe
The MYO7A-ZNF512 Fusion FISH Probe is used to confirm a fusion of the MYO7A and ZNF512 genes. The fusion of the MYO7A and ZNF512 genes has been associated with Uterine Carcinosarcoma. 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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| MYO7A-ZNF512-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-RERE | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-REOR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-REGO | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-REGR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-REAQ | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-ORRE | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-OROR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-ORGO | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-ORAQ | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GORE | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GOOR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GOGO | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GOGR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GOAQ | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GRRE | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GROR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GRGO | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GRGR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-GRAQ | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-AQRE | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-AQOR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-AQGO | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-AQGR | 20 (40 μL) | 200 μL |
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| MYO7A-ZNF512-20-AQAQ | 20 (40 μL) | 200 μL |
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MYO7A Gene Summary
This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
Gene Name: Myosin VIIA
Chromosome: CHR11: 76839309 -76926286
Locus: 11q13.5
ZNF512 Gene Summary
This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012]
Gene Name: Zinc Finger Protein 512
Chromosome: CHR2: 27805892 -27845963
Locus: 2p23.3
Gene Diseases
The MYO7A ZNF512 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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