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Gene-specific Break Apart Probe-ASXL1

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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 Details

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

Order Sheet

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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