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| Catalog: | GBAFP-ACHE-00048 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ACHE). 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: | ACHE Gene-specific Break Apart Probe is designed to detect potential ACHE 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 | Acetylcholinesterase (Cartwright Blood Group) |
| Gene Summary [Provided by RefSeq] | Acetylcholinesterase hydrolyzes the neurotransmitter, acetylcholine at neuromuscular junctions and brain cholinergic synapses, and thus terminates signal transmission. It is also found on the red blood cell membranes, where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties, but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene, and the structural diversity in the gene products arises from alternative mRNA splicing, and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain, muscle and other tissues is the hydrophilic species, which forms disulfide-linked oligomers with collagenous, or lipid-containing structural subunits. The other, alternatively spliced form, expressed primarily in the erythroid tissues, differs at the C-terminal end, and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally. [provided by RefSeq, Jul 2008] |
| Gene Symbol | ACHE |
| Location | 7q22.1 |
| Chromosome | Chromosome7 |
| Coordinates | This gene maps to 100487614-100493541 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-ACHE-00048-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-ACHE-00048-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ACHE-00048-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ACHE-00048-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ACHE-00048-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-ACHE-00048-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-ACHE-00048-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-ACHE-00048-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ACHE-00048-REGR | 599nm;515nm | 580nm;491nm |
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