Gene-specific Copy Number Variation Probe-DBH
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| Catalog: |
CNVFP-DBH-03593 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DBH). 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: |
DBH Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DBH genes. This product achieves the purpose of detection by hybridizing with the DBH 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 |
Dopamine Beta-hydroxylase |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an oxidoreductase belonging to the copper type II, ascorbate-dependent monooxygenase family. The encoded protein, expressed in neuroscretory vesicles and chromaffin granules of the adrenal medulla, catalyzes the conversion of dopamine to norepinephrine, which functions as both a hormone and as the main neurotransmitter of the sympathetic nervous system. The enzyme encoded by this gene exists exists in both soluble and membrane-bound forms, depending on the absence or presence, respectively, of a signal peptide. Mutations in this gene cause dopamine beta-hydroxylate deficiency in human patients, characterized by deficits in autonomic and cardiovascular function, including hypotension and ptosis. Polymorphisms in this gene may play a role in a variety of psychiatric disorders. [provided by RefSeq, Aug 2017] |
| Gene Symbol |
DBH |
| Location |
9q34.2 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 136501484-136524466 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-DBH-03593-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DBH-03593-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DBH-03593-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DBH-03593-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DBH-03593-AQ |
467nm |
418nm |
|
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