Gene-specific Copy Number Variation Probe-ENSA
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Catalog: |
CNVFP-ENSA-04540 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ENSA). 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: |
ENSA Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ENSA genes. This product achieves the purpose of detection by hybridizing with the ENSA 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 |
Endosulfine Alpha |
Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to a highly conserved cAMP-regulated phosphoprotein (ARPP) family. This protein was identified as an endogenous ligand for the sulfonylurea receptor, ABCC8/SUR1. ABCC8 is the regulatory subunit of the ATP-sensitive potassium (KATP) channel, which is located on the plasma membrane of pancreatic beta cells and plays a key role in the control of insulin release from pancreatic beta cells. This protein is thought to be an endogenous regulator of KATP channels. In vitro studies have demonstrated that this protein modulates insulin secretion through the interaction with KATP channel, and this gene has been proposed as a candidate gene for type 2 diabetes. At least eight alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008] |
Gene Symbol |
ENSA |
Location |
1q21.3 |
Chromosome |
Chromosome1 |
Coordinates |
This gene maps to 150594598-150602098 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-ENSA-04540-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-ENSA-04540-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-ENSA-04540-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-ENSA-04540-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-ENSA-04540-AQ |
467nm |
418nm |
|
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