RAI1-PEX1 Fusion FISH Probe
The RAI1-PEX1 Fusion FISH Probe is used to confirm a fusion of the RAI1 and PEX1 genes. The fusion of the RAI1 and PEX1 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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| RAI1-PEX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-RERE | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-REOR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-REGO | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-REGR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-REAQ | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-ORRE | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-OROR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-ORGO | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GORE | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GOOR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GOGO | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GOGR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GRRE | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GROR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GRGO | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GRGR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-AQRE | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-AQOR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-AQGO | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-AQGR | 20 (40 μL) | 200 μL |
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| RAI1-PEX1-20-AQAQ | 20 (40 μL) | 200 μL |
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PEX1 Gene Summary
This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Name: Peroxisomal Biogenesis Factor 1
Chromosome: CHR7: 92116336 -92157845
Locus: 7q21.2
RAI1 Gene Summary
This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]
Gene Name: Retinoic Acid Induced 1
Chromosome: CHR17: 17584786 -17714765
Locus: 17p11.2
Gene Diseases
The RAI1 PEX1 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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