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Aminoacylase

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Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate).

Below are the list of possible Aminoacylase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Aminoacylase-1

 Aminoacylase-1 ELISA Kit
 Aminoacylase-1 Recombinant
 Aminoacylase-1 Antibody
Also known as Aminoacylase-1 (ACY-1) (N-acyl-L-amino-acid amidohydrolase).
ACY1: Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). Defects in ACY1 are the cause of aminoacylase-1 deficiency (ACY1D). ACY1D results in a metabolic disorder manifesting with encephalopathy, unspecific psychomotor delay, psychomotor delay with atrophy of the vermis and syringo
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myelia, marked muscular hypotonia or normal clinical features. Epileptic seizures are a frequent feature. All affected individuals exhibit markedly increased urinary excretion of several N-acetylated amino acids. Belongs to the peptidase M20A family.

Protein type: Amino Acid Metabolism - arginine and proline; EC 3.5.1.14; Hydrolase

Molecular Function: aminoacylase activity; zinc ion binding

Biological Process: peptide catabolic process; proteolysis
 Acy1 ELISA Kit
 Acy1 Recombinant
 Acy1 Antibody
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Aminoacylase-1A

 Aminoacylase-1A ELISA Kit
 Aminoacylase-1A Recombinant
 Aminoacylase-1A Antibody
Also known as Aminoacylase-1A (ACY-1A) (ACY IA) (N-acyl-L-amino-acid amidohydrolase).
ACY1: Involved in the hydrolysis of N-acylated or N-acetylated amino acids (except L-aspartate). Defects in ACY1 are the cause of aminoacylase-1 deficiency (ACY1D). ACY1D results in a metabolic disorder manifesting with encephalopathy, unspecific psychomotor delay, psychomotor delay with atrophy of the vermis
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and syringomyelia, marked muscular hypotonia or normal clinical features. Epileptic seizures are a frequent feature. All affected individuals exhibit markedly increased urinary excretion of several N-acetylated amino acids. Belongs to the peptidase M20A family.

Protein type: Amino Acid Metabolism - arginine and proline; EC 3.5.1.14; Hydrolase

Molecular Function: aminoacylase activity; zinc ion binding

Biological Process: peptide catabolic process; protein catabolic process
 Acy1a ELISA Kit
 Acy1a Recombinant
 Acy1a Antibody
 Acy1 ELISA Kit
 Acy1 Recombinant
 Acy1 Antibody
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Aminoacylase-1B

 Aminoacylase-1B ELISA Kit
 Aminoacylase-1B Recombinant
 Aminoacylase-1B Antibody
Also known as Aminoacylase-1B (ACY-1B) (ACY IB) (N-acyl-L-amino-acid amidohydrolase).
enzyme that displays aminoacylase and/or metallopeptidase functions; may be involved in amino acid metabolism [RGD, Feb 2006]
 Acy1b ELISA Kit
 Acy1b Recombinant
 Acy1b Antibody
 Acy1 ELISA Kit
 Acy1 Recombinant
 Acy1 Antibody
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