CONTACT SUPPORT
Online Inquiry
| Catalog: | GBAFP-SCN11A-07159 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SCN11A). 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: | SCN11A Gene-specific Break Apart Probe is designed to detect potential SCN11A 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 11 |
| Gene Summary [Provided by RefSeq] | Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is highly expressed in nociceptive neurons of dorsal root ganglia and trigeminal ganglia. It mediates brain-derived neurotrophic factor-evoked membrane depolarization and is a major effector of peripheral inflammatory pain hypersensitivity. Mutations in this gene have been associated with hereditary sensory and autonomic neuropathy type VII and familial episodic pain syndrome-3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2017] |
| Gene Symbol | SCN11A |
| Location | 3p22.2 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 38887259-38992052 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SCN11A-07159-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SCN11A-07159-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SCN11A-07159-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SCN11A-07159-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SCN11A-07159-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SCN11A-07159-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SCN11A-07159-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SCN11A-07159-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SCN11A-07159-REGR | 599nm;515nm | 580nm;491nm |
Other Products