NOS1AP-AHI1 Fusion FISH Probe
The NOS1AP-AHI1 Fusion FISH Probe is used to confirm a fusion of the NOS1AP and AHI1 genes. The fusion of the NOS1AP and AHI1 genes has been associated with Bladder Urothelial 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NOS1AP-AHI1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| NOS1AP-AHI1-20-AQAQ | 20 (40 μL) | 200 μL |
|
NOS1AP Gene Summary
This gene encodes a cytosolic protein that binds to the signaling molecule, neuronal nitric oxide synthase (nNOS). This protein has a C-terminal PDZ-binding domain that mediates interactions with nNOS and an N-terminal phosphotyrosine binding (PTB) domain that binds to the small monomeric G protein, Dexras1. Studies of the related mouse and rat proteins have shown that this protein functions as an adapter protein linking nNOS to specific targets, such as Dexras1 and the synapsins. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2009]
Gene Name: Nitric Oxide Synthase 1 Adaptor Protein
Chromosome: CHR1: 162039580 -162339813
Locus: 1q23.3
AHI1 Gene Summary
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
Gene Name: Abelson Helper Integration Site 1
Chromosome: CHR6: 135605109 -135818903
Locus: 6q23.3
Gene Diseases
The NOS1AP AHI1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|