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| Catalog: | GBAFP-SLC5A7-17203 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SLC5A7). 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: | SLC5A7 Gene-specific Break Apart Probe is designed to detect potential SLC5A7 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 | Solute Carrier Family 5 Member 7 |
| Gene Summary [Provided by RefSeq] | This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
| Gene Symbol | SLC5A7 |
| Location | 2q12.3 |
| Chromosome | Chromosome2 |
| Coordinates | This gene maps to 108602994-108630443 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SLC5A7-17203-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SLC5A7-17203-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SLC5A7-17203-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SLC5A7-17203-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SLC5A7-17203-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SLC5A7-17203-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SLC5A7-17203-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SLC5A7-17203-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SLC5A7-17203-REGR | 599nm;515nm | 580nm;491nm |
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