Gene-specific Copy Number Variation Probe-NRXN3
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| Catalog: |
CNVFP-NRXN3-14393 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (NRXN3). 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: |
NRXN3 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to NRXN3 genes. This product achieves the purpose of detection by hybridizing with the NRXN3 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 |
Neurexin 3 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of a family of proteins that function in the nervous system as receptors and cell adhesion molecules. Extensive alternative splicing and the use of alternative promoters results in multiple transcript variants and protein isoforms for this gene, but the full-length nature of many of these variants has not been determined. Transcripts that initiate from an upstream promoter encode alpha isoforms, which contain epidermal growth factor-like (EGF-like) sequences and laminin G domains. Transcripts initiating from the downstream promoter encode beta isoforms, which lack EGF-like sequences. Genetic variation at this locus has been associated with a range of behavioral phenotypes, including alcohol dependence and autism spectrum disorder. [provided by RefSeq, Dec 2012] |
| Gene Symbol |
NRXN3 |
| Location |
14q24.3-q31.1 |
| Chromosome |
Chromosome14 |
| Coordinates |
This gene maps to 78870092-80330760 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-NRXN3-14393-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-NRXN3-14393-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-NRXN3-14393-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-NRXN3-14393-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-NRXN3-14393-AQ |
467nm |
418nm |
|
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