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| Catalog: | GBAFP-FGF20-02623 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (FGF20). 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: | FGF20 Gene-specific Break Apart Probe is designed to detect potential FGF20 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 20 |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors 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 gene product is a secreted neurotrophic factor but lacks a typical signal peptide. It is expressed in normal brain, particularly the cerebellum, and may regulate central nervous system development and function. Homodimerization of this protein was shown to regulate its receptor binding activity and concentration gradient in the extracellular matrix. Genetic variations of this gene have been associated with Parkinson disease susceptibility. [provided by RefSeq, Oct 2009] |
| Gene Symbol | FGF20 |
| Location | 8p22 |
| Chromosome | Chromosome8 |
| Coordinates | This gene maps to 16850333-16859674 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-FGF20-02623-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-FGF20-02623-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-FGF20-02623-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-FGF20-02623-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-FGF20-02623-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-FGF20-02623-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-FGF20-02623-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-FGF20-02623-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-FGF20-02623-REGR | 599nm;515nm | 580nm;491nm |
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