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| Catalog: | GBAFP-NDUFB9-14942 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NDUFB9). 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: | NDUFB9 Gene-specific Break Apart Probe is designed to detect potential NDUFB9 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 | NADH:ubiquinone Oxidoreductase Subunit B9 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
| Gene Symbol | NDUFB9 |
| Location | 8q24.13 |
| Chromosome | Chromosome8 |
| Coordinates | This gene maps to 125551342-125562227 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-NDUFB9-14942-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-NDUFB9-14942-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NDUFB9-14942-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NDUFB9-14942-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NDUFB9-14942-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-NDUFB9-14942-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-NDUFB9-14942-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-NDUFB9-14942-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NDUFB9-14942-REGR | 599nm;515nm | 580nm;491nm |
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