DMD-LIX1L Fusion FISH Probe
The DMD-LIX1L Fusion FISH Probe is used to confirm a fusion of the DMD and LIX1L genes. The fusion of the DMD and LIX1L 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 |
|---|---|---|---|---|
| DMD-LIX1L-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-RERE | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-REOR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-REGO | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-REGR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-REAQ | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-ORRE | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-OROR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-ORGO | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-ORAQ | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GORE | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GOOR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GOGO | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GOAQ | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GROR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GRGR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-GRAQ | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-AQRE | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-AQGO | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-AQGR | 20 (40 μL) | 200 μL |
|
|
| DMD-LIX1L-20-AQAQ | 20 (40 μL) | 200 μL |
|
DMD Gene Summary
This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [provided by RefSeq, Dec 2016]
Gene Name: Dystrophin
Chromosome: CHRX: 31137344 -33357726
Locus: Xp21.2-p21.1
LIX1L Gene Summary
The Limb And CNS Expressed 1 Like (LIX1L) gene is located on chr1 :145477084-145499091 at 1q21.1.
Gene Name: Limb And CNS Expressed 1 Like
Chromosome: CHR1: 145477084 -145499091
Locus: 1q21.1
Gene Diseases
The DMD LIX1L Fusion has been associated with the following diseases:
| Disease Name |
|---|
| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|