Gene-specific Copy Number Variation Probe-KCNA5
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| Catalog: |
CNVFP-KCNA5-07827 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNA5). 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: |
KCNA5 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNA5 genes. This product achieves the purpose of detection by hybridizing with the KCNA5 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 A Member 5 |
| Gene Summary [Provided by RefSeq] |
Potassium channels represent the most complex class of voltage-gated ino channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shaker-related subfamily. This member contains six membrane-spanning domains with a shaker-type repeat in the fourth segment. It belongs to the delayed rectifier class, the function of which could restore the resting membrane potential of beta cells after depolarization and thereby contribute to the regulation of insulin secretion. This gene is intronless, and the gene is clustered with genes KCNA1 and KCNA6 on chromosome 12. Defects in this gene are a cause of familial atrial fibrillation type 7 (ATFB7). [provided by RefSeq, May 2012] |
| Gene Symbol |
KCNA5 |
| Location |
12p13.32 |
| Chromosome |
Chromosome12 |
| Coordinates |
This gene maps to 5153084-5155949 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-KCNA5-07827-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-KCNA5-07827-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-KCNA5-07827-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-KCNA5-07827-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-KCNA5-07827-AQ |
467nm |
418nm |
|
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