RARS2-IP6K3 Fusion FISH Probe
The RARS2-IP6K3 Fusion FISH Probe is used to confirm a fusion of the RARS2 and IP6K3 genes. The fusion of the RARS2 and IP6K3 genes has been associated with Liver Hepatocellular 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 |
|---|---|---|---|---|
| RARS2-IP6K3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-RERE | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-REOR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-REGO | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-REGR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-OROR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GORE | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GROR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| RARS2-IP6K3-20-AQAQ | 20 (40 μL) | 200 μL |
|
RARS2 Gene Summary
This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Name: Arginyl-tRNA Synthetase 2, Mitochondrial
Chromosome: CHR6: 88224095 -88299735
Locus: 6q15
IP6K3 Gene Summary
This gene encodes a protein that belongs to the inositol phosphokinase (IPK) family. This protein is likely responsible for the conversion of inositol hexakisphosphate (InsP6) to diphosphoinositol pentakisphosphate (InsP7/PP-InsP5). It may also convert 1,3,4,5,6-pentakisphosphate (InsP5) to PP-InsP4. Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq, Dec 2008]
Gene Name: Inositol Hexakisphosphate Kinase 3
Chromosome: CHR6: 33689442 -33714762
Locus: 6p21.31
Gene Diseases
The RARS2 IP6K3 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|