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| Catalog: | GBAFP-NUB1-15171 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (NUB1). 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: | NUB1 Gene-specific Break Apart Probe is designed to detect potential NUB1 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 | Negative Regulator Of Ubiquitin Like Proteins 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011] |
| Gene Symbol | NUB1 |
| Location | 7q36.1 |
| Chromosome | Chromosome7 |
| Coordinates | This gene maps to 151038846-151075548 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-NUB1-15171-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-NUB1-15171-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-NUB1-15171-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-NUB1-15171-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-NUB1-15171-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-NUB1-15171-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-NUB1-15171-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-NUB1-15171-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-NUB1-15171-REGR | 599nm;515nm | 580nm;491nm |
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