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| Catalog: | GBAFP-SCN1A-07158 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SCN1A). 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: | SCN1A Gene-specific Break Apart Probe is designed to detect potential SCN1A 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 | Sodium Voltage-gated Channel Alpha Subunit 1 |
| Gene Summary [Provided by RefSeq] | Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015] |
| Gene Symbol | SCN1A |
| Location | 2q24.3 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 166845669-167005642 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SCN1A-07158-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SCN1A-07158-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SCN1A-07158-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SCN1A-07158-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SCN1A-07158-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SCN1A-07158-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SCN1A-07158-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SCN1A-07158-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SCN1A-07158-REGR | 599nm;515nm | 580nm;491nm |
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