Gene-specific Copy Number Variation Probe-AGT
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| Catalog: |
CNVFP-AGT-00347 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (AGT). 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: |
AGT Gene-specific copy number variation probes are mainly used to detect the copy number variation related to AGT genes. This product achieves the purpose of detection by hybridizing with the AGT 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 |
Angiotensinogen |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene, pre-angiotensinogen or angiotensinogen precursor, is expressed in the liver and is cleaved by the enzyme renin in response to lowered blood pressure. The resulting product, angiotensin I, is then cleaved by angiotensin converting enzyme (ACE) to generate the physiologically active enzyme angiotensin II. The protein is involved in maintaining blood pressure and in the pathogenesis of essential hypertension and preeclampsia. Mutations in this gene are associated with susceptibility to essential hypertension, and can cause renal tubular dysgenesis, a severe disorder of renal tubular development. Defects in this gene have also been associated with non-familial structural atrial fibrillation, and inflammatory bowel disease. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
AGT |
| Location |
1q42.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 230838271-230850336 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-AGT-00347-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-AGT-00347-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-AGT-00347-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-AGT-00347-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-AGT-00347-AQ |
467nm |
418nm |
|
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