C9ORF80-SNX30 Fusion FISH Probe
The C9ORF80-SNX30 Fusion FISH Probe is used to confirm a fusion of the C9ORF80 and SNX30 genes. The fusion of the C9ORF80 and SNX30 genes has been associated with Skin Cutaneous Melanoma. 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 |
|---|---|---|---|---|
| C9ORF80-SNX30-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-RERE | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-REOR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-REGO | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-REGR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-OROR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GORE | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GROR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| C9ORF80-SNX30-20-AQAQ | 20 (40 μL) | 200 μL |
|
SNX30 Gene Summary
The Sorting Nexin Family Member 30 (SNX30) gene is located on chr9 :115513133-115637267 at 9q32.
Gene Name: Sorting Nexin Family Member 30
Chromosome: CHR9: 115513133 -115637267
Locus: 9q32
Gene Diseases
The C9ORF80 SNX30 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|