DNM1L-CAP2 Fusion FISH Probe
The DNM1L-CAP2 Fusion FISH Probe is used to confirm a fusion of the DNM1L and CAP2 genes. The fusion of the DNM1L and CAP2 genes has been associated with Brain Lower Grade Glioma. 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 |
|---|---|---|---|---|
| DNM1L-CAP2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-RERE | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-REOR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-REGO | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-REGR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-OROR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GORE | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GROR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| DNM1L-CAP2-20-AQAQ | 20 (40 μL) | 200 μL |
|
DNM1L Gene Summary
This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]
Gene Name: Dynamin 1 Like
Chromosome: CHR12: 32832136 -32898584
Locus: 12p11.21
CAP2 Gene Summary
This gene was identified by its similarity to the gene for human adenylyl cyclase-associated protein. The function of the protein encoded by this gene is unknown. However, the protein appears to be able to interact with adenylyl cyclase-associated protein and actin. [provided by RefSeq, Jul 2008]
Gene Name: Cyclase Associated Actin Cytoskeleton Regulatory Protein 2
Chromosome: CHR6: 17393735 -17558023
Locus: 6p22.3
Gene Diseases
The DNM1L CAP2 Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|