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| Catalog: | GBAFP-TAB2-17960 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (TAB2). 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: | TAB2 Gene-specific Break Apart Probe is designed to detect potential TAB2 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 | TGF-beta Activated Kinase 1/MAP3K7 Binding Protein 2 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is an activator of MAP3K7/TAK1, which is required for for the IL-1 induced activation of nuclear factor kappaB and MAPK8/JNK. This protein forms a kinase complex with TRAF6, MAP3K7 and TAB1, and it thus serves as an adaptor that links MAP3K7 and TRAF6. This protein, along with TAB1 and MAP3K7, also participates in the signal transduction induced by TNFSF11/RANKl through the activation of the receptor activator of NF-kappaB (TNFRSF11A/RANK), which may regulate the development and function of osteoclasts. Studies of the related mouse protein indicate that it functions to protect against liver damage caused by chemical stressors. Mutations in this gene cause congenital heart defects, multiple types, 2 (CHTD2). Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014] |
| Gene Symbol | TAB2 |
| Location | 6q25.1 |
| Chromosome | Chromosome6 |
| Coordinates | This gene maps to 149639435-149732747 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-TAB2-17960-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-TAB2-17960-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-TAB2-17960-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-TAB2-17960-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-TAB2-17960-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-TAB2-17960-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-TAB2-17960-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-TAB2-17960-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-TAB2-17960-REGR | 599nm;515nm | 580nm;491nm |
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