Gene-specific Copy Number Variation Probe-SCN1A
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| Catalog: |
CNVFP-SCN1A-18102 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SCN1A). 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: |
SCN1A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SCN1A genes. This product achieves the purpose of detection by hybridizing with the SCN1A 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 Alpha Subunit 1 |
| Gene Summary [Provided by RefSeq] |
Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015] |
| Gene Symbol |
SCN1A |
| Location |
2q24.3 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 166845669-167005642 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-SCN1A-18102-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SCN1A-18102-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SCN1A-18102-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SCN1A-18102-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SCN1A-18102-AQ |
467nm |
418nm |
|
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