Gene-specific Copy Number Variation Probe-CNTNAP2
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| Catalog: |
CNVFP-CNTNAP2-02881 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CNTNAP2). 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: |
CNTNAP2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CNTNAP2 genes. This product achieves the purpose of detection by hybridizing with the CNTNAP2 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 |
Contactin Associated Protein Like 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the neurexin family which functions in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, thrombospondin N-terminal-like domains and a putative PDZ binding site. This protein is localized at the juxtaparanodes of myelinated axons, and mediates interactions between neurons and glia during nervous system development and is also involved in localization of potassium channels within differentiating axons. This gene encompasses almost 1.5% of chromosome 7 and is one of the largest genes in the human genome. It is directly bound and regulated by forkhead box protein P2, a transcription factor related to speech and language development. This gene has been implicated in multiple neurodevelopmental disorders, including Gilles de la Tourette syndrome, schizophrenia, epilepsy, autism, ADHD and intellectual disability. [provided by RefSeq, Jul 2017] |
| Gene Symbol |
CNTNAP2 |
| Location |
7q35-q36.1 |
| Chromosome |
Chromosome7 |
| Coordinates |
This gene maps to 145813452-148118088 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-CNTNAP2-02881-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CNTNAP2-02881-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CNTNAP2-02881-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CNTNAP2-02881-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CNTNAP2-02881-AQ |
467nm |
418nm |
|
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