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| Catalog: | GBAFP-SAG-16779 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SAG). 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: | SAG Gene-specific Break Apart Probe is designed to detect potential SAG 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 | S-antigen Visual Arrestin |
| Gene Summary [Provided by RefSeq] | Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness. [provided by RefSeq, Jul 2008] |
| Gene Symbol | SAG |
| Location | 2q37.1 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 234216308-234255701 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SAG-16779-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SAG-16779-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SAG-16779-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SAG-16779-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SAG-16779-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SAG-16779-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SAG-16779-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SAG-16779-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SAG-16779-REGR | 599nm;515nm | 580nm;491nm |
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