Gene-specific Copy Number Variation Probe-ATP2A1
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| Catalog: |
CNVFP-ATP2A1-01253 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (ATP2A1). 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: |
ATP2A1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to ATP2A1 genes. This product achieves the purpose of detection by hybridizing with the ATP2A1 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 Sarcoplasmic/endoplasmic Reticulum Ca2+ Transporting 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Oct 2013] |
| Gene Symbol |
ATP2A1 |
| Location |
16p11.2 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 28889808-28915830 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-ATP2A1-01253-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-ATP2A1-01253-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-ATP2A1-01253-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-ATP2A1-01253-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-ATP2A1-01253-AQ |
467nm |
418nm |
|
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