Gene-specific Copy Number Variation Probe-KCNJ6
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| Catalog: |
CNVFP-KCNJ6-07779 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNJ6). 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: |
KCNJ6 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNJ6 genes. This product achieves the purpose of detection by hybridizing with the KCNJ6 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 J Member 6 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015] |
| Gene Symbol |
KCNJ6 |
| Location |
21q22.13 |
| Chromosome |
Chromosome21 |
| Coordinates |
This gene maps to 38996785-39288696 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-KCNJ6-07779-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNJ6-07779-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNJ6-07779-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNJ6-07779-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNJ6-07779-AQ |
467nm |
418nm |
|
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