Gene-specific Copy Number Variation Probe-SCN1B
Add to Cart
| Catalog: |
CNVFP-SCN1B-18101 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SCN1B). 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: |
SCN1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SCN1B genes. This product achieves the purpose of detection by hybridizing with the SCN1B 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 |
Sodium Voltage-gated Channel Beta Subunit 1 |
| Gene Summary [Provided by RefSeq] |
Voltage-gated sodium channels are heteromeric proteins that function in the generation and propagation of action potentials in muscle and neuronal cells. They are composed of one alpha and two beta subunits, where the alpha subunit provides channel activity and the beta-1 subunit modulates the kinetics of channel inactivation. This gene encodes a sodium channel beta-1 subunit. Mutations in this gene result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009] |
| Gene Symbol |
SCN1B |
| Location |
19q13.11 |
| Chromosome |
Chromosome19 |
| Coordinates |
This gene maps to 35521591-35531353 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-SCN1B-18101-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SCN1B-18101-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SCN1B-18101-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SCN1B-18101-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SCN1B-18101-AQ |
467nm |
418nm |
|
Other Products
