C2CD3-SYTL1 Fusion FISH Probe
The C2CD3-SYTL1 Fusion FISH Probe is used to confirm a fusion of the C2CD3 and SYTL1 genes. The fusion of the C2CD3 and SYTL1 genes has been associated with Ovarian Serous Cystadenocarcinoma. 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 |
|---|---|---|---|---|
| C2CD3-SYTL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| C2CD3-SYTL1-20-AQAQ | 20 (40 μL) | 200 μL |
|
C2CD3 Gene Summary
This gene encodes a protein that functions as a regulator of centriole elongation. Studies of the orthologous mouse protein show that it promotes centriolar distal appendage assembly and is also required for the recruitment of other ciliogenic proteins, including intraflagellar transport proteins. Mutations in this gene cause orofaciodigital syndrome XIV (OFD14), a ciliopathy resulting in malformations of the oral cavity, face and digits. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]
Gene Name: C2 Calcium Dependent Domain Containing 3
Chromosome: CHR11: 73745479 -73882064
Locus: 11q13.4
SYTL1 Gene Summary
The Synaptotagmin Like 1 (SYTL1) gene is located on chr1 :27668482-27680423 at 1p36.11.
Gene Name: Synaptotagmin Like 1
Chromosome: CHR1: 27668482 -27680423
Locus: 1p36.11
Gene Diseases
The C2CD3 SYTL1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Ovarian Serous Cystadenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|