Gene-specific Copy Number Variation Probe-EDN3
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| Catalog: |
CNVFP-EDN3-04451 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (EDN3). 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: |
EDN3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to EDN3 genes. This product achieves the purpose of detection by hybridizing with the EDN3 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 |
Endothelin 3 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the endothelin family. Endothelins are endothelium-derived vasoactive peptides involved in a variety of biological functions. The active form of this protein is a 21 amino acid peptide processed from the precursor protein. The active peptide is a ligand for endothelin receptor type B (EDNRB). The interaction of this endothelin with EDNRB is essential for development of neural crest-derived cell lineages, such as melanocytes and enteric neurons. Mutations in this gene and EDNRB have been associated with Hirschsprung disease (HSCR) and Waardenburg syndrome (WS), which are congenital disorders involving neural crest-derived cells. Altered expression of this gene is implicated in tumorigenesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014] |
| Gene Symbol |
EDN3 |
| Location |
20q13.32 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 57875498-57901047 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-EDN3-04451-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-EDN3-04451-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-EDN3-04451-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-EDN3-04451-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-EDN3-04451-AQ |
467nm |
418nm |
|
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