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| Catalog: | GBAFP-TNFSF12-18252 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNFSF12). 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: | TNFSF12 Gene-specific Break Apart Probe is designed to detect potential TNFSF12 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 12 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein is a ligand for the FN14/TWEAKR receptor. This cytokine has overlapping signaling functions with TNF, but displays a much wider tissue distribution. This cytokine, which exists in both membrane-bound and secreted forms, can induce apoptosis via multiple pathways of cell death in a cell type-specific manner. This cytokine is also found to promote proliferation and migration of endothelial cells, and thus acts as a regulator of angiogenesis. Alternative splicing results in multiple transcript variants. Some transcripts skip the last exon of this gene and continue into the second exon of the neighboring TNFSF13 gene; such read-through transcripts are contained in GeneID 407977, TNFSF12-TNFSF13. [provided by RefSeq, Oct 2010] |
| Gene Symbol | TNFSF12 |
| Location | 17p13.1 |
| Chromosome | Chromosome17 |
| Coordinates | This gene maps to 7452374-7461207 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TNFSF12-18252-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TNFSF12-18252-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TNFSF12-18252-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TNFSF12-18252-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TNFSF12-18252-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TNFSF12-18252-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TNFSF12-18252-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TNFSF12-18252-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TNFSF12-18252-REGR | 599nm;515nm | 580nm;491nm |
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