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| Catalog: | GBAFP-RGR-16496 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (RGR). 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: | RGR Gene-specific Break Apart Probe is designed to detect potential RGR 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 | Retinal G Protein Coupled Receptor |
| Gene Summary [Provided by RefSeq] | This gene encodes a putative retinal G-protein coupled receptor. The gene is a member of the opsin subfamily of the 7 transmembrane, G-protein coupled receptor 1 family. Like other opsins which bind retinaldehyde, it contains a conserved lysine residue in the seventh transmembrane domain. The protein acts as a photoisomerase to catalyze the conversion of all-trans-retinal to 11-cis-retinal. The reverse isomerization occurs with rhodopsin in retinal photoreceptor cells. The protein is exclusively expressed in tissue adjacent to retinal photoreceptor cells, the retinal pigment epithelium and Mueller cells. This gene may be associated with autosomal recessive and autosomal dominant retinitis pigmentosa (arRP and adRP, respectively). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
| Gene Symbol | RGR |
| Location | 10q23.1 |
| Chromosome | Chromosome10 |
| Coordinates | This gene maps to 86004808-86018944 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-RGR-16496-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-RGR-16496-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-RGR-16496-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-RGR-16496-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-RGR-16496-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-RGR-16496-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-RGR-16496-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-RGR-16496-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-RGR-16496-REGR | 599nm;515nm | 580nm;491nm |
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