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| Catalog: | GBAFP-SPN-17610 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SPN). 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: | SPN Gene-specific Break Apart Probe is designed to detect potential SPN 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 | Sialophorin |
| Gene Summary [Provided by RefSeq] | This gene encodes a highly sialylated glycoprotein that functions in antigen-specific activation of T cells, and is found on the surface of thymocytes, T lymphocytes, monocytes, granulocytes, and some B lymphocytes. It contains a mucin-like extracellular domain, a transmembrane region and a carboxy-terminal intracellular region. The extracellular domain has a high proportion of serine and threonine residues, allowing extensive O-glycosylation, and has one potential N-glycosylation site, while the carboxy-terminal region has potential phosphorylation sites that may mediate transduction of activation signals. Different glycoforms of this protein have been described. In stimulated immune cells, proteolytic cleavage of the extracellular domain occurs in some cell types, releasing a soluble extracellular fragment. Defects in expression of this gene are associated with Wiskott-Aldrich syndrome. [provided by RefSeq, Sep 2017] |
| Gene Symbol | SPN |
| Location | 16p11.2 |
| Chromosome | Chromosome16 |
| Coordinates | This gene maps to 29674299-29681823 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SPN-17610-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SPN-17610-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SPN-17610-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SPN-17610-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SPN-17610-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SPN-17610-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SPN-17610-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SPN-17610-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SPN-17610-REGR | 599nm;515nm | 580nm;491nm |
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