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| Catalog: | GBAFP-RTTN-07112 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RTTN). 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: | RTTN Gene-specific Break Apart Probe is designed to detect potential RTTN 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 | Rotatin |
| Gene Summary [Provided by RefSeq] | This gene encodes a large protein whose specific function is unknown. Absence of the orthologous protein in mouse results in embryonic lethality with deficient axial rotation, abnormal differentiation of the neural tube, and randomized looping of the heart tube during development. In human, mutations in this gene are associated with polymicrogyria with seizures. In human fibroblasts this protein localizes at the ciliary basal bodies. Given the intracellular localization of this protein and the phenotypic effects of mutations, this gene is suspected of playing a role in the maintenance of normal ciliary structure which in turn effects the developmental process of left-right organ specification, axial rotation, and perhaps notochord development. [provided by RefSeq, Jan 2013] |
| Gene Symbol | RTTN |
| Location | 18q22.2 |
| Chromosome | Chromosome18 |
| Coordinates | This gene maps to 67671042-67872962 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-RTTN-07112-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-RTTN-07112-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RTTN-07112-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RTTN-07112-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RTTN-07112-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-RTTN-07112-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-RTTN-07112-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-RTTN-07112-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RTTN-07112-REGR | 599nm;515nm | 580nm;491nm |
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