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| Catalog: | GBAFP-AXIN2-00590 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (AXIN2). 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: | AXIN2 Gene-specific Break Apart Probe is designed to detect potential AXIN2 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 | Axin 2 |
| Gene Summary [Provided by RefSeq] | The Axin-related protein, Axin2, presumably plays an important role in the regulation of the stability of beta-catenin in the Wnt signaling pathway, like its rodent homologs, mouse conductin/rat axil. In mouse, conductin organizes a multiprotein complex of APC (adenomatous polyposis of the colon), beta-catenin, glycogen synthase kinase 3-beta, and conductin, which leads to the degradation of beta-catenin. Apparently, the deregulation of beta-catenin is an important event in the genesis of a number of malignancies. The AXIN2 gene has been mapped to 17q23-q24, a region that shows frequent loss of heterozygosity in breast cancer, neuroblastoma, and other tumors. Mutations in this gene have been associated with colorectal cancer with defective mismatch repair. [provided by RefSeq, Jul 2008] |
| Gene Symbol | AXIN2 |
| Location | 17q24.1 |
| Chromosome | Chromosome17 |
| Coordinates | This gene maps to 63524682-63557740 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-AXIN2-00590-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-AXIN2-00590-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-AXIN2-00590-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-AXIN2-00590-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-AXIN2-00590-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-AXIN2-00590-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-AXIN2-00590-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-AXIN2-00590-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-AXIN2-00590-REGR | 599nm;515nm | 580nm;491nm |
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