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| Catalog: | GBAFP-FGF12-02649 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (FGF12). 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: | FGF12 Gene-specific Break Apart Probe is designed to detect potential FGF12 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 | Fibroblast Growth Factor 12 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. Two alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
| Gene Symbol | FGF12 |
| Location | 3q28-q29 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 191857181-192445388 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-FGF12-02649-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-FGF12-02649-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-FGF12-02649-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-FGF12-02649-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-FGF12-02649-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-FGF12-02649-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-FGF12-02649-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-FGF12-02649-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-FGF12-02649-REGR | 599nm;515nm | 580nm;491nm |
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