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| Catalog: | GBAFP-ACY1-09671 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (ACY1). 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: | ACY1 Gene-specific Break Apart Probe is designed to detect potential ACY1 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 | Aminoacylase 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Nov 2010] |
| Gene Symbol | ACY1 |
| Location | 3p21.2 |
| Chromosome | Chromosome3 |
| Coordinates | This gene maps to 52017299-52023218 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | OR; GR | GBAFP-ACY1-09671-ORGR | 573nm;515nm | 548nm;491nm | |
| 2 | AQ; OR | GBAFP-ACY1-09671-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-ACY1-09671-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-ACY1-09671-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-ACY1-09671-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; OR | GBAFP-ACY1-09671-GROR | 515nm;573nm | 491nm;548nm | |
| 7 | GR; RE | GBAFP-ACY1-09671-GRRE | 515nm;599nm | 491nm;580nm | |
| 8 | RE; GO | GBAFP-ACY1-09671-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-ACY1-09671-REGR | 599nm;515nm | 580nm;491nm |
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