Gene-specific Copy Number Variation Probe-SCN11A
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| Catalog: |
CNVFP-SCN11A-18098 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SCN11A). 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: |
SCN11A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SCN11A genes. This product achieves the purpose of detection by hybridizing with the SCN11A 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 11 |
| Gene Summary [Provided by RefSeq] |
Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is highly expressed in nociceptive neurons of dorsal root ganglia and trigeminal ganglia. It mediates brain-derived neurotrophic factor-evoked membrane depolarization and is a major effector of peripheral inflammatory pain hypersensitivity. Mutations in this gene have been associated with hereditary sensory and autonomic neuropathy type VII and familial episodic pain syndrome-3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2017] |
| Gene Symbol |
SCN11A |
| Location |
3p22.2 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 38887259-38992052 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-SCN11A-18098-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SCN11A-18098-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SCN11A-18098-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SCN11A-18098-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SCN11A-18098-AQ |
467nm |
418nm |
|
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