Gene-specific Copy Number Variation Probe-KCNQ4
Add to Cart
Catalog: |
CNVFP-KCNQ4-07806 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNQ4). 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: |
KCNQ4 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNQ4 genes. This product achieves the purpose of detection by hybridizing with the KCNQ4 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 4 |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene forms a potassium channel that is thought to play a critical role in the regulation of neuronal excitability, particularly in sensory cells of the cochlea. The current generated by this channel is inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. The encoded protein can form a homomultimeric potassium channel or possibly a heteromultimeric channel in association with the protein encoded by the KCNQ3 gene. Defects in this gene are a cause of nonsyndromic sensorineural deafness type 2 (DFNA2), an autosomal dominant form of progressive hearing loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Gene Symbol |
KCNQ4 |
Location |
1p34.2 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 41249683-41306124 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-KCNQ4-07806-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-KCNQ4-07806-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-KCNQ4-07806-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-KCNQ4-07806-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-KCNQ4-07806-AQ |
467nm |
418nm |
|
Other Products