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| Catalog: | GBAFP-DCLK2-11386 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (DCLK2). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | DCLK2 Gene-specific Break Apart Probe is designed to detect potential DCLK2 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| 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 |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-DCLK2-11386-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-DCLK2-11386-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-DCLK2-11386-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-DCLK2-11386-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-DCLK2-11386-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-DCLK2-11386-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-DCLK2-11386-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-DCLK2-11386-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-DCLK2-11386-REGR | 599nm;515nm | 580nm;491nm |
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