Gene-specific Copy Number Variation Probe-ENG
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| Catalog: |
CNVFP-ENG-04562 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ENG). 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: |
ENG Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ENG genes. This product achieves the purpose of detection by hybridizing with the ENG 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 |
Endoglin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013] |
| Gene Symbol |
ENG |
| Location |
9q34.11 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 130577290-130617047 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-ENG-04562-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ENG-04562-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ENG-04562-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ENG-04562-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ENG-04562-AQ |
467nm |
418nm |
|
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