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| Catalog: | GBAFP-ASXL1-10113 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ASXL1). 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: | ASXL1 Gene-specific Break Apart Probe is designed to detect potential ASXL1 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 | Additional Sex Combs Like 1, Transcriptional Regulator |
| Gene Summary [Provided by RefSeq] | This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009] |
| Gene Symbol | ASXL1 |
| Location | 20q11.21 |
| Chromosome | Chromosome20 |
| Coordinates | This gene maps to 30946146-31027122 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-ASXL1-10113-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-ASXL1-10113-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ASXL1-10113-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ASXL1-10113-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ASXL1-10113-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-ASXL1-10113-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-ASXL1-10113-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-ASXL1-10113-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ASXL1-10113-REGR | 599nm;515nm | 580nm;491nm |
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