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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 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 |
| 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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