Gene-specific Copy Number Variation Probe-SYN2
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| Catalog: |
CNVFP-SYN2-20256 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SYN2). 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: |
SYN2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SYN2 genes. This product achieves the purpose of detection by hybridizing with the SYN2 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 II |
| 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. This member of the synapsin family encodes a neuron-specific phosphoprotein that selectively binds to small synaptic vesicles in the presynaptic nerve terminal. Polymorphisms in this gene are associated with abnormal presynaptic function and related neuronal disorders, including autism, epilepsy, bipolar disorder and schizophrenia. Alternative splicing of this gene results in multiple transcript variants. The tissue inhibitor of metalloproteinase 4 gene is located within an intron of this gene and is transcribed in the opposite direction. [provided by RefSeq, Feb 2014] |
| Gene Symbol |
SYN2 |
| Location |
3p25.2 |
| Chromosome |
Chromosome3 |
| Coordinates |
This gene maps to 12045861-12233532 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-SYN2-20256-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SYN2-20256-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SYN2-20256-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SYN2-20256-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SYN2-20256-AQ |
467nm |
418nm |
|
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