IFT81-INSR Fusion FISH Probe
The IFT81-INSR Fusion FISH Probe is used to confirm a fusion of the IFT81 and INSR genes. The fusion of the IFT81 and INSR 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 |
|---|---|---|---|---|
| IFT81-INSR-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-RERE | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-REOR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-REGO | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-REGR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-OROR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GORE | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GROR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| IFT81-INSR-20-AQAQ | 20 (40 μL) | 200 μL |
|
INSR Gene Summary
This gene encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form a heterotetrameric receptor. Binding of insulin or other ligands to this receptor activates the insulin signaling pathway, which regulates glucose uptake and release, as well as the synthesis and storage of carbohydrates, lipids and protein. Mutations in this gene underlie the inherited severe insulin resistance syndromes including type A insulin resistance syndrome, Donohue syndrome and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]
Gene Name: Insulin Receptor
Chromosome: CHR19: 7112265 -7294011
Locus: 19p13.2
IFT81 Gene Summary
The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]
Gene Name: Intraflagellar Transport 81
Chromosome: CHR12: 110562139 -110656600
Locus: 12q24.11
Gene Diseases
The IFT81 INSR Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|