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| Catalog: | GBAFP-SNX15-17571 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SNX15). 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: | SNX15 Gene-specific Break Apart Probe is designed to detect potential SNX15 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 | Sorting Nexin 15 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010] |
| Gene Symbol | SNX15 |
| Location | 11q13.1 |
| Chromosome | Chromosome11 |
| Coordinates | This gene maps to 64794879-64808044 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-SNX15-17571-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-SNX15-17571-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SNX15-17571-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SNX15-17571-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SNX15-17571-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-SNX15-17571-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-SNX15-17571-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-SNX15-17571-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SNX15-17571-REGR | 599nm;515nm | 580nm;491nm |
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