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Gene-specific Break Apart Probe-ACY1

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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 Details

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

Order Sheet

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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