OLFM2-CECR2 Fusion FISH Probe
The OLFM2-CECR2 Fusion FISH Probe is used to confirm a fusion of the OLFM2 and CECR2 genes. The fusion of the OLFM2 and CECR2 genes has been associated with Uterine Carcinosarcoma. 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 |
|---|---|---|---|---|
| OLFM2-CECR2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| OLFM2-CECR2-20-AQAQ | 20 (40 μL) | 200 μL |
|
CECR2 Gene Summary
This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]
Gene Name: CECR2, Histone Acetyl-lysine Reader
Chromosome: CHR22: 17956627 -18033845
Locus: 22q11.1-q11.21
OLFM2 Gene Summary
The Olfactomedin 2 (OLFM2) gene is located on chr19 :9964393-10047070 at 19p13.2.
Gene Name: Olfactomedin 2
Chromosome: CHR19: 9964393 -10047070
Locus: 19p13.2
Gene Diseases
The OLFM2 CECR2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|