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| Catalog: | GBAFP-KCNT1-13335 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (KCNT1). 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: | KCNT1 Gene-specific Break Apart Probe is designed to detect potential KCNT1 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 | Potassium Sodium-activated Channel Subfamily T Member 1 |
| Gene Summary [Provided by RefSeq] | Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
| Gene Symbol | KCNT1 |
| Location | 9q34.3 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 138594030-138684993 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-KCNT1-13335-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-KCNT1-13335-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-KCNT1-13335-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-KCNT1-13335-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-KCNT1-13335-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-KCNT1-13335-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-KCNT1-13335-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-KCNT1-13335-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-KCNT1-13335-REGR | 599nm;515nm | 580nm;491nm |
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