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| Catalog: | GBAFP-SNX13-07804 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (SNX13). 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: | SNX13 Gene-specific Break Apart Probe is designed to detect potential SNX13 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 13 |
| Gene Summary [Provided by RefSeq] | This gene encodes a PHOX domain- and RGS domain-containing protein that belongs to the sorting nexin (SNX) family and the regulator of G protein signaling (RGS) family. The PHOX domain is a phosphoinositide binding domain, and the SNX family members are involved in intracellular trafficking. The RGS family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. The RGS domain of this protein interacts with G alpha(s), accelerates its GTP hydrolysis, and attenuates G alpha(s)-mediated signaling. Overexpression of this protein delayes lysosomal degradation of the epidermal growth factor receptor. Because of its bifunctional role, this protein may link heterotrimeric G protein signaling and vesicular trafficking. [provided by RefSeq, Jul 2008] |
| Gene Symbol | SNX13 |
| Location | 7p21.1 |
| Chromosome | Chromosome7 |
| Coordinates | This gene maps to 17830384-17980131 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-SNX13-07804-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-SNX13-07804-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-SNX13-07804-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-SNX13-07804-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-SNX13-07804-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-SNX13-07804-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-SNX13-07804-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-SNX13-07804-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-SNX13-07804-REGR | 599nm;515nm | 580nm;491nm |
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