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Gene-specific Break Apart Probe-HEXB

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Catalog: GBAFP-HEXB-12746
Classification: Gene-specific Break Apart Probes
Description: Our Gene-specific Break Apart Probes usually target the flanks of the target gene (HEXB). 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: HEXB Gene-specific Break Apart Probe is designed to detect potential HEXB 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 Hexosaminidase Subunit Beta
Gene Summary [Provided by RefSeq] Hexosaminidase B is the beta subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Beta subunit gene mutations lead to Sandhoff disease (GM2-gangliosidosis type II). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]
Gene Symbol HEXB
Location 5q13.3
Chromosome Chromosome5
Coordinates This gene maps to 73980968-74017113 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR; GR GBAFP-HEXB-12746-ORGR 573nm;515nm 548nm;491nm
2 AQ; OR GBAFP-HEXB-12746-AQOR 467nm;573nm 418nm;548nm
3 GO; GR GBAFP-HEXB-12746-GOGR 551nm;515nm 525nm;491nm
4 GO; RE GBAFP-HEXB-12746-GORE 551nm;599nm 525nm;580nm
5 GR; GO GBAFP-HEXB-12746-GRGO 515nm;551nm 491nm;525nm
6 GR; OR GBAFP-HEXB-12746-GROR 515nm;573nm 491nm;548nm
7 GR; RE GBAFP-HEXB-12746-GRRE 515nm;599nm 491nm;580nm
8 RE; GO GBAFP-HEXB-12746-REGO 599nm;551nm 580nm;525nm
9 RE; GR GBAFP-HEXB-12746-REGR 599nm;515nm 580nm;491nm

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