Gene-specific Copy Number Variation Probe-PRKAG2
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Catalog: |
CNVFP-PRKAG2-16297 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (PRKAG2). 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: |
PRKAG2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to PRKAG2 genes. This product achieves the purpose of detection by hybridizing with the PRKAG2 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 |
Protein Kinase AMP-activated Non-catalytic Subunit Gamma 2 |
Gene Summary [Provided by RefSeq] |
AMP-activated protein kinase (AMPK) is a heterotrimeric protein composed of a catalytic alpha subunit, a noncatalytic beta subunit, and a noncatalytic regulatory gamma subunit. Various forms of each of these subunits exist, encoded by different genes. AMPK is an important energy-sensing enzyme that monitors cellular energy status and functions by inactivating key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This gene is a member of the AMPK gamma subunit family. Mutations in this gene have been associated with Wolff-Parkinson-White syndrome, familial hypertrophic cardiomyopathy, and glycogen storage disease of the heart. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jan 2015] |
Gene Symbol |
PRKAG2 |
Location |
7q36.1 |
Chromosome |
Chromosome7 |
Coordinates |
This gene maps to 151253200-151574316 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-PRKAG2-16297-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-PRKAG2-16297-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-PRKAG2-16297-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-PRKAG2-16297-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-PRKAG2-16297-AQ |
467nm |
418nm |
|
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