RAI1-IFT20 Fusion FISH Probe
The RAI1-IFT20 Fusion FISH Probe is used to confirm a fusion of the RAI1 and IFT20 genes. The fusion of the RAI1 and IFT20 genes has been associated with Lung Squamous 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 |
|---|---|---|---|---|
| RAI1-IFT20-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-RERE | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-REOR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-REGO | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-REGR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-OROR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GORE | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GROR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| RAI1-IFT20-20-AQAQ | 20 (40 μL) | 200 μL |
|
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
IFT20 Gene Summary
This gene encodes a intraflagellar transport protein important for intracellular transport. The encoded protein forms part of a complex involved in trafficking of proteins from the Golgi body, including recycling of immune signalling components (Finetti et al., PubMed: 19855387). This gene is part of a complex set of sense-antisense loci that may be co-regulated. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome 14.[provided by RefSeq, Jun 2012]
Gene Name: Intraflagellar Transport 20
Chromosome: CHR17: 26655352 -26662495
Locus: 17q11.2
Gene Diseases
The RAI1 IFT20 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|