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| Catalog: | GBAFP-TNFSF13-18251 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNFSF13). 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: | TNFSF13 Gene-specific Break Apart Probe is designed to detect potential TNFSF13 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 13 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the tumor necrosis factor (TNF) ligand family. This protein is a ligand for TNFRSF17/BCMA, a member of the TNF receptor family. This protein and its receptor are both found to be important for B cell development. In vitro experiments suggested that this protein may be able to induce apoptosis through its interaction with other TNF receptor family proteins such as TNFRSF6/FAS and TNFRSF14/HVEM. Alternative splicing results in multiple transcript variants. Some transcripts that skip the last exon of the upstream gene (TNFSF12) and continue into the second exon of this gene have been identified; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
| Gene Symbol | TNFSF13 |
| Location | 17p13.1 |
| Chromosome | Chromosome17 |
| Coordinates | This gene maps to 7461608-7464925 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TNFSF13-18251-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TNFSF13-18251-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TNFSF13-18251-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TNFSF13-18251-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TNFSF13-18251-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TNFSF13-18251-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TNFSF13-18251-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TNFSF13-18251-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TNFSF13-18251-REGR | 599nm;515nm | 580nm;491nm |
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