CNKSR3-PLP1 Fusion FISH Probe
The CNKSR3-PLP1 Fusion FISH Probe is used to confirm a fusion of the CNKSR3 and PLP1 genes. The fusion of the CNKSR3 and PLP1 genes has been associated with Sarcoma. 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 |
|---|---|---|---|---|
| CNKSR3-PLP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-RERE | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-REOR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-REGO | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-REGR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-OROR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GORE | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GROR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| CNKSR3-PLP1-20-AQAQ | 20 (40 μL) | 200 μL |
|
PLP1 Gene Summary
This gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein may play a role in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause Pelizaeus-Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants, including the DM20 splice variant. [provided by RefSeq, Feb 2015]
Gene Name: Proteolipid Protein 1
Chromosome: CHRX: 103031438 -103047547
Locus: Xq22.2
CNKSR3 Gene Summary
The CNKSR Family Member 3 (CNKSR3) gene is located on chr6 :154726432-154831753 at 6q25.2.
Gene Name: CNKSR Family Member 3
Chromosome: CHR6: 154726432 -154831753
Locus: 6q25.2
Gene Diseases
The CNKSR3 PLP1 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|