Gene-specific Copy Number Variation Probe-DCLK2
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| Catalog: |
CNVFP-DCLK2-03569 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DCLK2). 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: |
DCLK2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DCLK2 genes. This product achieves the purpose of detection by hybridizing with the DCLK2 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 Like Kinase 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the protein kinase superfamily and the doublecortin family. The protein encoded by this gene contains two N-terminal doublecortin domains, which bind microtubules and regulate microtubule polymerization, a C-terminal serine/threonine protein kinase domain, which shows substantial homology to Ca2+/calmodulin-dependent protein kinase, and a serine/proline-rich domain in between the doublecortin and the protein kinase domains, which mediates multiple protein-protein interactions. The microtubule-polymerizing activity of the encoded protein is independent of its protein kinase activity. Mouse studies show that the DCX gene, another family member, and this gene share function in the establishment of hippocampal organization and that their absence results in a severe epileptic phenotype and lethality, as described in human patients with lissencephaly. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Sep 2010] |
| Gene Symbol |
DCLK2 |
| Location |
4q31.23-q31.3 |
| Chromosome |
Chromosome4 |
| Coordinates |
This gene maps to 150999425-151178608 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-DCLK2-03569-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DCLK2-03569-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DCLK2-03569-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DCLK2-03569-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DCLK2-03569-AQ |
467nm |
418nm |
|
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