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| Catalog: | GBAFP-SPTBN2-07948 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SPTBN2). 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: | SPTBN2 Gene-specific Break Apart Probe is designed to detect potential SPTBN2 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 | Spectrin Beta, Non-erythrocytic 2 |
| Gene Summary [Provided by RefSeq] | Spectrins are principle components of a cell's membrane-cytoskeleton and are composed of two alpha and two beta spectrin subunits. The protein encoded by this gene (SPTBN2), is called spectrin beta non-erythrocytic 2 or beta-III spectrin. It is related to, but distinct from, the beta-II spectrin gene which is also known as spectrin beta non-erythrocytic 1 (SPTBN1). SPTBN2 regulates the glutamate signaling pathway by stabilizing the glutamate transporter EAAT4 at the surface of the plasma membrane. Mutations in this gene cause a form of spinocerebellar ataxia, SCA5, that is characterized by neurodegeneration, progressive locomotor incoordination, dysarthria, and uncoordinated eye movements. [provided by RefSeq, Dec 2009] |
| Gene Symbol | SPTBN2 |
| Location | 11q13.2 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 66452719-66488870 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SPTBN2-07948-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SPTBN2-07948-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SPTBN2-07948-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SPTBN2-07948-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SPTBN2-07948-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SPTBN2-07948-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SPTBN2-07948-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SPTBN2-07948-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SPTBN2-07948-REGR | 599nm;515nm | 580nm;491nm |
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