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Recombinant ACY1/Aminoacylase-1 Monoclonal Antibody (AN300343P)

Recombinant ACY1/Aminoacylase-1 Monoclonal Antibody - 1
  • Recombinant ACY1/Aminoacylase-1 Monoclonal Antibody - 1
  • Recombinant ACY1/Aminoacylase-1 Monoclonal Antibody - 2
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100μL $ 380.00
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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.
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Unconjugated

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