Gene-specific Copy Number Variation Probe-SYN3
Add to Cart
| Catalog: |
CNVFP-SYN3-20257 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SYN3). 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: |
SYN3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SYN3 genes. This product achieves the purpose of detection by hybridizing with the SYN3 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 |
Synapsin III |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the synapsin gene family. Synapsins encode neuronal phosphoproteins which associate with the cytoplasmic surface of synaptic vesicles. Family members are characterized by common protein domains, and they are implicated in synaptogenesis and the modulation of neurotransmitter release, suggesting a potential role in several neuropsychiatric diseases. The protein encoded by this gene shares the synapsin family domain model, with domains A, C, and E exhibiting the highest degree of conservation. The protein contains a unique domain J, located between domains C and E. Based on this gene's localization to 22q12.3, a possible schizophrenia susceptibility locus, and the established neurobiological roles of the synapsins, this family member may represent a candidate gene for schizophrenia. The TIMP3 gene is located within an intron of this gene and is transcribed in the opposite direction. Alternative splicing of this gene results in multiple splice variants that encode different isoforms. [provided by RefSeq, Oct 2008] |
| Gene Symbol |
SYN3 |
| Location |
22q12.3 |
| Chromosome |
Chromosome22 |
| Coordinates |
This gene maps to 32908539-33454377 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-SYN3-20257-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SYN3-20257-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SYN3-20257-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SYN3-20257-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SYN3-20257-AQ |
467nm |
418nm |
|
Other Products
