Gene-specific Copy Number Variation Probe-WDR19
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| Catalog: |
CNVFP-WDR19-23083 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (WDR19). 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: |
WDR19 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to WDR19 genes. This product achieves the purpose of detection by hybridizing with the WDR19 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 |
WD Repeat Domain 19 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
WDR19 |
| Location |
4p14 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 39184023-39287430 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-WDR19-23083-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-WDR19-23083-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-WDR19-23083-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-WDR19-23083-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-WDR19-23083-AQ |
467nm |
418nm |
|
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