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| Catalog: | GBAFP-FGD4-12172 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (FGD4). 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: | FGD4 Gene-specific Break Apart Probe is designed to detect potential FGD4 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 | FYVE, RhoGEF And PH Domain Containing 4 |
| Gene Summary [Provided by RefSeq] | This gene encodes a protein that is involved in the regulation of the actin cytoskeleton and cell shape. This protein contains an actin filament-binding domain, which together with its Dbl homology domain and one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-binding domain, and it is also involved in the activation of CDC42 via the exchange of bound GDP for free GTP. The activation of CDC42 also enables this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2015] |
| Gene Symbol | FGD4 |
| Location | 12p11.21 |
| Chromosome | Chromosome12 |
| Coordinates | This gene maps to 32655040-32798984 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-FGD4-12172-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-FGD4-12172-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-FGD4-12172-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-FGD4-12172-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-FGD4-12172-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-FGD4-12172-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-FGD4-12172-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-FGD4-12172-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-FGD4-12172-REGR | 599nm;515nm | 580nm;491nm |
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