ACOT7-PLEKHG5 Fusion FISH Probe
The ACOT7-PLEKHG5 Fusion FISH Probe is used to confirm a fusion of the ACOT7 and PLEKHG5 genes. The fusion of the ACOT7 and PLEKHG5 genes has been associated with Esophageal 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 |
|---|---|---|---|---|
| ACOT7-PLEKHG5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-RERE | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-REOR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-REGO | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-REGR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-OROR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GORE | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GROR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| ACOT7-PLEKHG5-20-AQAQ | 20 (40 μL) | 200 μL |
|
ACOT7 Gene Summary
This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008]
Gene Name: Acyl-CoA Thioesterase 7
Chromosome: CHR1: 6324331 -6453826
Locus: 1p36.31
PLEKHG5 Gene Summary
This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
Gene Name: Pleckstrin Homology And RhoGEF Domain Containing G5
Chromosome: CHR1: 6526151 -6580069
Locus: 1p36.31
Gene Diseases
The ACOT7 PLEKHG5 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Esophageal Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|