FBF1-ACOX1 Fusion FISH Probe
The FBF1-ACOX1 Fusion FISH Probe is used to confirm a fusion of the FBF1 and ACOX1 genes. The fusion of the FBF1 and ACOX1 genes has been associated with Kidney Renal Papillary Cell Carcinoma. 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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| FBF1-ACOX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-RERE | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-REOR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-REGO | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-REGR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-REAQ | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-ORRE | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-OROR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-ORGO | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GORE | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GOOR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GOGO | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GOGR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GRRE | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GROR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GRGO | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GRGR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-AQRE | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-AQOR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-AQGO | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-AQGR | 20 (40 μL) | 200 μL |
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| FBF1-ACOX1-20-AQAQ | 20 (40 μL) | 200 μL |
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ACOX1 Gene Summary
The protein encoded by this gene is the first enzyme of the fatty acid beta-oxidation pathway, which catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. It donates electrons directly to molecular oxygen, thereby producing hydrogen peroxide. Defects in this gene result in pseudoneonatal adrenoleukodystrophy, a disease that is characterized by accumulation of very long chain fatty acids. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Name: Acyl-CoA Oxidase 1
Chromosome: CHR17: 73937588 -73975515
Locus: 17q25.1
FBF1 Gene Summary
The Fas Binding Factor 1 (FBF1) gene is located on chr17 :73906617-73937119 at 17q25.1.
Gene Name: Fas Binding Factor 1
Chromosome: CHR17: 73906617 -73937119
Locus: 17q25.1
Gene Diseases
The FBF1 ACOX1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Papillary Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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