Gene-specific Copy Number Variation Probe-KCNT1
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| Catalog: |
CNVFP-KCNT1-07797 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNT1). 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: |
KCNT1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNT1 genes. This product achieves the purpose of detection by hybridizing with the KCNT1 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 |
Potassium Sodium-activated Channel Subfamily T Member 1 |
| Gene Summary [Provided by RefSeq] |
Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
| Gene Symbol |
KCNT1 |
| Location |
9q34.3 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 138594030-138684993 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-KCNT1-07797-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNT1-07797-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNT1-07797-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNT1-07797-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNT1-07797-AQ |
467nm |
418nm |
|
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