Recombinant ACY1/Aminoacylase-1 Monoclonal Antibody (AN300343P)

For research use only.
Verified Samples | Verified Samples in IHC: Human kidney |
Dilution | IHC-P 1:100-1:500 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human |
Applications | IHC-P |
Clonality | Monoclonal |
Immunogen | Recombinant Human ACY1/Aminoacylase-1 protein |
Abbre | ACY1 |
Synonyms | HEL-S, ACY, ACY1, ACY-1, ACY1D, HEL-S-5 |
Swissprot | |
Tissue Specificity | Expression is highest in kidney, strong in brain and weaker in placenta and spleen. |
Concentration | 1 mg/mL |
Buffer | 0.2 μm filtered solution in PBS |
Purification Method | Protein A |
Research Areas | Signal Transduction, Metabolism |
Clone No. | 6G15 |
Conjugation | Unconjugated |
Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
Shipping | Ice bag |
background | 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. |
Other Clones
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Unconjugated
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