Gene-specific Copy Number Variation Probe-ATP8A2
Add to Cart
| Catalog: |
CNVFP-ATP8A2-01205 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ATP8A2). 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: |
ATP8A2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ATP8A2 genes. This product achieves the purpose of detection by hybridizing with the ATP8A2 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 |
ATPase Phospholipid Transporting 8A2 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the P4 ATPase family of proteins, which are thought to be involved in a process called lipid flipping, whereby phospholipids are translocated inwards from the exoplasmic leaflet to the cytosolic leaflet of the cell membrane, which aids in generating and maintaining asymmetry in membrane lipids. This protein is predicted to contain an E1 E2 ATPase, a haloacid dehalogenase-like hydrolase (HAD) domain, and multiple transmembrane domains. Associations between this protein and cell cycle control protein 50A are important for translocation of phosphatidylserine across membranes. Mutations in this gene have been associated with a syndrome (CAMRQ4) characterized by cerebellar ataxia and cognitive disabilities. In addition, a translocation breakpoint within this gene was observed in an individual with neurological dysfunction. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
ATP8A2 |
| Location |
13q12.13 |
| Chromosome |
Chromosome13 |
| Coordinates |
This gene maps to 25946208-26595420 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-ATP8A2-01205-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ATP8A2-01205-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ATP8A2-01205-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ATP8A2-01205-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ATP8A2-01205-AQ |
467nm |
418nm |
|
Other Products
