Gene-specific Copy Number Variation Probe-WASHC5
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| Catalog: |
CNVFP-WASHC5-23145 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WASHC5). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
WASHC5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WASHC5 genes. This product achieves the purpose of detection by hybridizing with the WASHC5 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
WASH Complex Subunit 5 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq, Aug 2009] |
| Gene Symbol |
WASHC5 |
| Location |
8q24.13 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 125091818-125024259 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-WASHC5-23145-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WASHC5-23145-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WASHC5-23145-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WASHC5-23145-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WASHC5-23145-AQ |
467nm |
418nm |
|
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