Gene-specific Copy Number Variation Probe-STX1B
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| Catalog: |
CNVFP-STX1B-20052 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (STX1B). 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: |
STX1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to STX1B genes. This product achieves the purpose of detection by hybridizing with the STX1B 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 |
Syntaxin 1B |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene belongs to a family of proteins thought to play a role in the exocytosis of synaptic vesicles. Vesicle exocytosis releases vesicular contents and is important to various cellular functions. For instance, the secretion of transmitters from neurons plays an important role in synaptic transmission. After exocytosis, the membrane and proteins from the vesicle are retrieved from the plasma membrane through the process of endocytosis. Mutations in this gene have been identified as one cause of fever-associated epilepsy syndromes. A possible link between this gene and Parkinson's disease has also been suggested. [provided by RefSeq, Jan 2015] |
| Gene Symbol |
STX1B |
| Location |
16p11.2 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 31000576-31021829 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-STX1B-20052-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-STX1B-20052-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-STX1B-20052-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-STX1B-20052-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-STX1B-20052-AQ |
467nm |
418nm |
|
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