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| Catalog: | GBAFP-TNFRSF13C-08528 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TNFRSF13C). 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: | TNFRSF13C Gene-specific Break Apart Probe is designed to detect potential TNFRSF13C 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 Receptor Superfamily Member 13C |
| Gene Summary [Provided by RefSeq] | B cell-activating factor (BAFF) enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. Overexpression of Baff in mice results in mature B-cell hyperplasia and symptoms of systemic lupus erythematosus (SLE). Also, some SLE patients have increased levels of BAFF in serum. Therefore, it has been proposed that abnormally high levels of BAFF may contribute to the pathogenesis of autoimmune diseases by enhancing the survival of autoreactive B cells. The protein encoded by this gene is a receptor for BAFF and is a type III transmembrane protein containing a single extracellular cysteine-rich domain. It is thought that this receptor is the principal receptor required for BAFF-mediated mature B-cell survival. [provided by RefSeq, Jul 2008] |
| Gene Symbol | TNFRSF13C |
| Location | 22q13.2 |
| Chromosome | Chromosome22 |
| Coordinates | This gene maps to 42321035-42322821 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-TNFRSF13C-08528-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-TNFRSF13C-08528-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TNFRSF13C-08528-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TNFRSF13C-08528-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TNFRSF13C-08528-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-TNFRSF13C-08528-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-TNFRSF13C-08528-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-TNFRSF13C-08528-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TNFRSF13C-08528-REGR | 599nm;515nm | 580nm;491nm |
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