Gene-specific Copy Number Variation Probe-KCNQ2
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| Catalog: |
CNVFP-KCNQ2-07804 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNQ2). 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: |
KCNQ2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNQ2 genes. This product achieves the purpose of detection by hybridizing with the KCNQ2 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 Voltage-gated Channel Subfamily Q Member 2 |
| Gene Summary [Provided by RefSeq] |
The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
KCNQ2 |
| Location |
20q13.33 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 62037541-62103993 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-KCNQ2-07804-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNQ2-07804-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNQ2-07804-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNQ2-07804-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNQ2-07804-AQ |
467nm |
418nm |
|
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