Gene-specific Copy Number Variation Probe-WNT11
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| Catalog: |
CNVFP-WNT11-22987 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WNT11). 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: |
WNT11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WNT11 genes. This product achieves the purpose of detection by hybridizing with the WNT11 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 11 |
| 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 encodes a protein which shows 97%, 85%, and 63% amino acid identity with mouse, chicken, and Xenopus Wnt11 protein, respectively. This gene may play roles in the development of skeleton, kidney and lung, and is considered to be a plausible candidate gene for High Bone Mass Syndrome. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
WNT11 |
| Location |
11q13.5 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 75897369-75917574 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-WNT11-22987-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WNT11-22987-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WNT11-22987-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WNT11-22987-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WNT11-22987-AQ |
467nm |
418nm |
|
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