Gene-specific Copy Number Variation Probe-WNT1
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| Catalog: |
CNVFP-WNT1-22988 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WNT1). 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: |
WNT1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WNT1 genes. This product achieves the purpose of detection by hybridizing with the WNT1 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 1 |
| 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. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
WNT1 |
| Location |
12q13.12 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 49372235-49376396 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-WNT1-22988-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WNT1-22988-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WNT1-22988-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WNT1-22988-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WNT1-22988-AQ |
467nm |
418nm |
|
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