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| Catalog: | GBAFP-TNFSF11-18254 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNFSF11). 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: | TNFSF11 Gene-specific Break Apart Probe is designed to detect potential TNFSF11 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 | TNF Superfamily Member 11 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the tumor necrosis factor (TNF) cytokine family which is a ligand for osteoprotegerin and functions as a key factor for osteoclast differentiation and activation. This protein was shown to be a dentritic cell survival factor and is involved in the regulation of T cell-dependent immune response. T cell activation was reported to induce expression of this gene and lead to an increase of osteoclastogenesis and bone loss. This protein was shown to activate antiapoptotic kinase AKT/PKB through a signaling complex involving SRC kinase and tumor necrosis factor receptor-associated factor (TRAF) 6, which indicated this protein may have a role in the regulation of cell apoptosis. Targeted disruption of the related gene in mice led to severe osteopetrosis and a lack of osteoclasts. The deficient mice exhibited defects in early differentiation of T and B lymphocytes, and failed to form lobulo-alveolar mammary structures during pregnancy. Two alternatively spliced transcript variants have been found. [provided by RefSeq, Jul 2008] |
| Gene Symbol | TNFSF11 |
| Location | 13q14.11 |
| Chromosome | Chromosome13 |
| Coordinates | This gene maps to 43136871-43182149 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TNFSF11-18254-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TNFSF11-18254-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TNFSF11-18254-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TNFSF11-18254-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TNFSF11-18254-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TNFSF11-18254-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TNFSF11-18254-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TNFSF11-18254-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TNFSF11-18254-REGR | 599nm;515nm | 580nm;491nm |
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