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| Catalog: | GBAFP-OPN1MW-15259 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (OPN1MW). 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: | OPN1MW Gene-specific Break Apart Probe is designed to detect potential OPN1MW 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 | Opsin 1, Medium Wave Sensitive |
| Gene Summary [Provided by RefSeq] | This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009] |
| Gene Symbol | OPN1MW |
| Location | Xq28 |
| Chromosome | ChromosomeX |
| Coordinates | This gene maps to 153485202-153499470 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-OPN1MW-15259-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-OPN1MW-15259-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-OPN1MW-15259-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-OPN1MW-15259-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-OPN1MW-15259-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-OPN1MW-15259-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-OPN1MW-15259-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-OPN1MW-15259-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-OPN1MW-15259-REGR | 599nm;515nm | 580nm;491nm |
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