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| Catalog: | GBAFP-COQ6-11147 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (COQ6). 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: | COQ6 Gene-specific Break Apart Probe is designed to detect potential COQ6 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 | Coenzyme Q6, Monooxygenase |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene belongs to the ubiH/COQ6 family. It is an evolutionarily conserved monooxygenase required for the biosynthesis of coenzyme Q10 (or ubiquinone), which is an essential component of the mitochondrial electron transport chain, and one of the most potent lipophilic antioxidants implicated in the protection of cell damage by reactive oxygen species. Knockdown of this gene in mouse and zebrafish results in decreased growth due to increased apoptosis. Mutations in this gene are associated with autosomal recessive coenzyme Q10 deficiency-6 (COQ10D6), which manifests as nephrotic syndrome with sensorineural deafness. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2012] |
| Gene Symbol | COQ6 |
| Location | 14q24.3 |
| Chromosome | Chromosome14 |
| Coordinates | This gene maps to 74416636-74429813 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-COQ6-11147-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-COQ6-11147-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-COQ6-11147-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-COQ6-11147-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-COQ6-11147-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-COQ6-11147-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-COQ6-11147-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-COQ6-11147-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-COQ6-11147-REGR | 599nm;515nm | 580nm;491nm |
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