Gene-specific Copy Number Variation Probe-WNT5A
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| Catalog: |
CNVFP-WNT5A-22980 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WNT5A). 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: |
WNT5A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WNT5A genes. This product achieves the purpose of detection by hybridizing with the WNT5A 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 |
Wnt Family Member 5A |
| Gene Summary [Provided by RefSeq] |
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene encodes a member of the WNT family that signals through both the canonical and non-canonical WNT pathways. This protein is a ligand for the seven transmembrane receptor frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012] |
| Gene Symbol |
WNT5A |
| Location |
3p14.3 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 55499742-55521331 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-WNT5A-22980-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WNT5A-22980-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WNT5A-22980-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WNT5A-22980-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WNT5A-22980-AQ |
467nm |
418nm |
|
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