CCDC22-ZNF673 Fusion FISH Probe
The CCDC22-ZNF673 Fusion FISH Probe is used to confirm a fusion of the CCDC22 and ZNF673 genes. The fusion of the CCDC22 and ZNF673 genes has been associated with Prostate Adenocarcinoma. 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 |
|---|---|---|---|---|
| CCDC22-ZNF673-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-RERE | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-REOR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-REGO | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-REGR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-OROR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GORE | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GROR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| CCDC22-ZNF673-20-AQAQ | 20 (40 μL) | 200 μL |
|
CCDC22 Gene Summary
This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]
Gene Name: Coiled-coil Domain Containing 22
Chromosome: CHRX: 49091926 -49106987
Locus: Xp11.23
Gene Diseases
The CCDC22 ZNF673 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|