Gene-specific Copy Number Variation Probe-SNTA1
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| Catalog: |
CNVFP-SNTA1-19496 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNTA1). 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: |
SNTA1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNTA1 genes. This product achieves the purpose of detection by hybridizing with the SNTA1 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 |
Syntrophin Alpha 1 |
| Gene Summary [Provided by RefSeq] |
Syntrophins are cytoplasmic peripheral membrane scaffold proteins that are components of the dystrophin-associated protein complex. This gene is a member of the syntrophin gene family and encodes the most common syntrophin isoform found in cardiac tissues. The N-terminal PDZ domain of this syntrophin protein interacts with the C-terminus of the pore-forming alpha subunit (SCN5A) of the cardiac sodium channel Nav1.5. This protein also associates cardiac sodium channels with the nitric oxide synthase-PMCA4b (plasma membrane Ca-ATPase subtype 4b) complex in cardiomyocytes. This gene is a susceptibility locus for Long-QT syndrome (LQT) - an inherited disorder associated with sudden cardiac death from arrhythmia - and sudden infant death syndrome (SIDS). This protein also associates with dystrophin and dystrophin-related proteins at the neuromuscular junction and alters intracellular calcium ion levels in muscle tissue. [provided by RefSeq, Jan 2013] |
| Gene Symbol |
SNTA1 |
| Location |
20q11.21 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 31995762-32031698 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-SNTA1-19496-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SNTA1-19496-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SNTA1-19496-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SNTA1-19496-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SNTA1-19496-AQ |
467nm |
418nm |
|
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