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| Catalog: | GBAFP-ABCA1-00102 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ABCA1). 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: | ABCA1 Gene-specific Break Apart Probe is designed to detect potential ABCA1 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 | ATP Binding Cassette Subfamily A Member 1 |
| Gene Summary [Provided by RefSeq] | The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in this gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency. [provided by RefSeq, Jul 2008] |
| Gene Symbol | ABCA1 |
| Location | 9q31.1 |
| Chromosome | Chromosome9 |
| Coordinates | This gene maps to 107543283-107690527 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-ABCA1-00102-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-ABCA1-00102-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ABCA1-00102-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ABCA1-00102-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ABCA1-00102-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-ABCA1-00102-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-ABCA1-00102-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-ABCA1-00102-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ABCA1-00102-REGR | 599nm;515nm | 580nm;491nm |
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