Gene-specific Copy Number Variation Probe-SNTG1
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| Catalog: |
CNVFP-SNTG1-19495 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SNTG1). 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: |
SNTG1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SNTG1 genes. This product achieves the purpose of detection by hybridizing with the SNTG1 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 Gamma 1 |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This family member plays a role in mediating gamma-enolase trafficking to the plasma membrane and in enhancing its neurotrophic activity. Mutations in this gene are associated with idiopathic scoliosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2016] |
| Gene Symbol |
SNTG1 |
| Location |
8q11.21 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 50824596-51705427 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-SNTG1-19495-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SNTG1-19495-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SNTG1-19495-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SNTG1-19495-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SNTG1-19495-AQ |
467nm |
418nm |
|
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