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| Catalog: | GBAFP-AP3M1-00318 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (AP3M1). 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: | AP3M1 Gene-specific Break Apart Probe is designed to detect potential AP3M1 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 | Adaptor Related Protein Complex 3 Mu 1 Subunit |
| Gene Summary [Provided by RefSeq] | The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane, and it may directly function in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
| Gene Symbol | AP3M1 |
| Location | 10q22.2 |
| Chromosome | Chromosome10 |
| Coordinates | This gene maps to 75880014-75910826 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-AP3M1-00318-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-AP3M1-00318-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-AP3M1-00318-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-AP3M1-00318-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-AP3M1-00318-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-AP3M1-00318-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-AP3M1-00318-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-AP3M1-00318-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-AP3M1-00318-REGR | 599nm;515nm | 580nm;491nm |
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