ACSF3-ZNF483 Fusion FISH Probe
The ACSF3-ZNF483 Fusion FISH Probe is used to confirm a fusion of the ACSF3 and ZNF483 genes. The fusion of the ACSF3 and ZNF483 genes has been associated with Sarcoma. 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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| ACSF3-ZNF483-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-RERE | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-REOR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-REGO | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-REGR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-REAQ | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-ORRE | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-OROR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-ORGO | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-ORAQ | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GORE | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GOOR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GOGO | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GOGR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GOAQ | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GRRE | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GROR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GRGO | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GRGR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-GRAQ | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-AQRE | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-AQOR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-AQGO | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-AQGR | 20 (40 μL) | 200 μL |
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| ACSF3-ZNF483-20-AQAQ | 20 (40 μL) | 200 μL |
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ZNF483 Gene Summary
The Zinc Finger Protein 483 (ZNF483) gene is located on chr9 :114287446-114340124 at 9q31.3.
Gene Name: Zinc Finger Protein 483
Chromosome: CHR9: 114287446 -114340124
Locus: 9q31.3
ACSF3 Gene Summary
This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Sep 2013]
Gene Name: Acyl-CoA Synthetase Family Member 3
Chromosome: CHR16: 89160216 -89222171
Locus: 16q24.3
Gene Diseases
The ACSF3 ZNF483 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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