Gene-specific Copy Number Variation Probe-KCNE3
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Catalog: |
CNVFP-KCNE3-07846 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (KCNE3). 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: |
KCNE3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to KCNE3 genes. This product achieves the purpose of detection by hybridizing with the KCNE3 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 E Regulatory Subunit 3 |
Gene Summary [Provided by RefSeq] |
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion 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. This gene encodes a member of the potassium channel, voltage-gated, isk-related subfamily. This member is a type I membrane protein, and a beta subunit that assembles with a potassium channel alpha-subunit to modulate the gating kinetics and enhance stability of the multimeric complex. This gene is prominently expressed in the kidney. A missense mutation in this gene is associated with hypokalemic periodic paralysis. [provided by RefSeq, Jul 2008] |
Gene Symbol |
KCNE3 |
Location |
11q13.4 |
Chromosome |
Chromosome11 |
Coordinates |
This gene maps to 74165885-74178600 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-KCNE3-07846-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-KCNE3-07846-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-KCNE3-07846-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-KCNE3-07846-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-KCNE3-07846-AQ |
467nm |
418nm |
|
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