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| Catalog: | GBAFP-PSEN2-16176 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (PSEN2). 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: | PSEN2 Gene-specific Break Apart Probe is designed to detect potential PSEN2 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 | Presenilin 2 |
| Gene Summary [Provided by RefSeq] | Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1 or PSEN2) or the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor such that, they either directly regulate gamma-secretase activity, or themselves act are protease enzymes. Two alternatively spliced transcript variants encoding different isoforms of PSEN2 have been identified. [provided by RefSeq, Jul 2008] |
| Gene Symbol | PSEN2 |
| Location | 1q42.13 |
| Chromosome | Chromosome1 |
| Coordinates | This gene maps to 227058272-227083804 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-PSEN2-16176-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-PSEN2-16176-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-PSEN2-16176-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-PSEN2-16176-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-PSEN2-16176-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-PSEN2-16176-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-PSEN2-16176-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-PSEN2-16176-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-PSEN2-16176-REGR | 599nm;515nm | 580nm;491nm |
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