Gene-specific Copy Number Variation Probe-KCNJ11
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| Catalog: |
CNVFP-KCNJ11-07808 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNJ11). 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: |
KCNJ11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNJ11 genes. This product achieves the purpose of detection by hybridizing with the KCNJ11 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 11 |
| Gene Summary [Provided by RefSeq] |
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2009] |
| Gene Symbol |
KCNJ11 |
| Location |
11p15.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 17406795-17410878 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-KCNJ11-07808-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNJ11-07808-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNJ11-07808-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNJ11-07808-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNJ11-07808-AQ |
467nm |
418nm |
|
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