Gene-specific Copy Number Variation Probe-DCX
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| Catalog: |
CNVFP-DCX-03544 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DCX). 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: |
DCX Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DCX genes. This product achieves the purpose of detection by hybridizing with the DCX 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 |
Doublecortin |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the doublecortin family. The protein encoded by this gene is a cytoplasmic protein and contains two doublecortin domains, which bind microtubules. In the developing cortex, cortical neurons must migrate over long distances to reach the site of their final differentiation. The encoded protein appears to direct neuronal migration by regulating the organization and stability of microtubules. In addition, the encoded protein interacts with LIS1, the regulatory gamma subunit of platelet activating factor acetylhydrolase, and this interaction is important to proper microtubule function in the developing cortex. Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex, leading to epilepsy, cognitive disability, subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain" syndrome) in males. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2010] |
| Gene Symbol |
DCX |
| Location |
Xq23 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 110537006-110655460 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-DCX-03544-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DCX-03544-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DCX-03544-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DCX-03544-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DCX-03544-AQ |
467nm |
418nm |
|
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