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| Catalog: | GBAFP-AUH-00584 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (AUH). 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: | AUH Gene-specific Break Apart Probe is designed to detect potential AUH 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 | AU RNA Binding Methylglutaconyl-CoA Hydratase |
| Gene Summary [Provided by RefSeq] | This gene encodes bifunctional mitochondrial protein that has both RNA-binding and hydratase activities. The encoded protein is a methylglutaconyl-CoA hydratase that catalyzes the hydration of 3-methylglutaconyl-CoA to 3-hydroxy-3-methyl-glutaryl-CoA, a critical step in the leucine degradation pathway. This protein also binds AU-rich elements (AREs) found in the 3' UTRs of rapidly decaying mRNAs including c-fos, c-myc and granulocyte/ macrophage colony stimulating factor. ARE elements are involved in directing RNA to rapid degradation and deadenylation. This protein is localizes to the mitochondrial matrix and the inner mitochondrial membrane and may be involved in mitochondrial protein synthesis. Mutations in this gene are the cause of 3-methylglutaconic aciduria, type I. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
| Gene Symbol | AUH |
| Location | 9q22.31 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 93976096-94124206 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-AUH-00584-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-AUH-00584-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-AUH-00584-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-AUH-00584-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-AUH-00584-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-AUH-00584-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-AUH-00584-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-AUH-00584-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-AUH-00584-REGR | 599nm;515nm | 580nm;491nm |
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