Gene-specific Copy Number Variation Probe-WNT4
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| Catalog: |
CNVFP-WNT4-22979 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WNT4). 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: |
WNT4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WNT4 genes. This product achieves the purpose of detection by hybridizing with the WNT4 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 4 |
| 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 is a member of the WNT gene family, and is the first signaling molecule shown to influence the sex-determination cascade. It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat. This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation. This gene and another two family members, WNT2 and WNT7B, may be associated with abnormal proliferation in breast tissue. Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
WNT4 |
| Location |
1p36.12 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 22443797-22469519 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-WNT4-22979-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WNT4-22979-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WNT4-22979-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WNT4-22979-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WNT4-22979-AQ |
467nm |
418nm |
|
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