Gene-specific Copy Number Variation Probe-KCNQ3
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| Catalog: |
CNVFP-KCNQ3-07802 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNQ3). 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: |
KCNQ3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNQ3 genes. This product achieves the purpose of detection by hybridizing with the KCNQ3 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 3 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein that functions in the regulation of neuronal excitability. The encoded protein forms an M-channel by associating with the products of the related KCNQ2 or KCNQ5 genes, which both encode integral membrane proteins. M-channel currents are inhibited by M1 muscarinic acetylcholine receptors and are activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 2 (BFNC2), also known as epilepsy, benign neonatal type 2 (EBN2). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2014] |
| Gene Symbol |
KCNQ3 |
| Location |
8q24.22 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 133133104-133493004 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-KCNQ3-07802-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNQ3-07802-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNQ3-07802-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNQ3-07802-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNQ3-07802-AQ |
467nm |
418nm |
|
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