CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-RPE65-06957 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RPE65). 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: | RPE65 Gene-specific Break Apart Probe is designed to detect potential RPE65 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 | RPE65, Retinoid Isomerohydrolase |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a component of the vitamin A visual cycle of the retina which supplies the 11-cis retinal chromophore of the photoreceptors opsin visual pigments. It is a member of the carotenoid cleavage oxygenase superfamily. All members of this superfamily are non-heme iron oxygenases with a seven-bladed propeller fold and oxidatively cleave carotenoid carbon:carbon double bonds. However, the protein encoded by this gene has acquired a divergent function that involves the concerted O-alkyl ester cleavage of its all-trans retinyl ester substrate and all-trans to 11-cis double bond isomerization of the retinyl moiety. As such, it performs the essential enzymatic isomerization step in the synthesis of 11-cis retinal. Mutations in this gene are associated with early-onset severe blinding disorders such as Leber congenital. [provided by RefSeq, Oct 2017] |
| Gene Symbol | RPE65 |
| Location | 1p31.3 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 68894506-68915642 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-RPE65-06957-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-RPE65-06957-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RPE65-06957-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RPE65-06957-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RPE65-06957-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-RPE65-06957-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-RPE65-06957-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-RPE65-06957-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RPE65-06957-REGR | 599nm;515nm | 580nm;491nm |
Other Products