Full Product Name
Rat Acy1a Polyclonal Antibody
Product Synonym Names
Acy1; ACY IA; N-acyl-L-amino-acid amidohydrolase
Product Gene Name
anti-ACY1A antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q6AYS7
Purity/Purification
Immunogen Affinity Purified
Form/Format
Liquid; 0.1MxPBS, 50% Glycerol, pH7.5
Concentration
200 ug/ml (lot specific)
Immunogen
Recombinant Human Acy1a Protein
Preparation and Storage
Store at 4 degree C for frequent use. Store at -20 degree C to -70 degree C for 6 months.
Other Notes
Small volumes of anti-ACY1A antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-ACY1A antibody
Western Blot (WB), Immunohistochemistry (IHC)
NCBI/Uniprot data below describe general gene information for ACY1A. It may not necessarily be applicable to this product.
NCBI GenBank Nucleotide #
NP_001005383.1
[Other Products]
UniProt Primary Accession #
Q6AYS7
[Other Products]
UniProt Related Accession #
Q6AYS7; Q6PTT0[Other Products]
NCBI Official Full Name
aminoacylase-1A
NCBI Official Synonym Full Names
aminoacylase 1
NCBI Official Symbol
Acy1 [Similar Products]
NCBI Official Synonym Symbols
Acy1a; Acy1b
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NCBI Protein Information
aminoacylase-1A
UniProt Protein Name
Aminoacylase-1A
UniProt Synonym Protein Names
ACY IA; N-acyl-L-amino-acid amidohydrolase
Protein Family
Aminoacylase
UniProt Gene Name
Acy1a [Similar Products]
UniProt Synonym Gene Names
Acy1; ACY-1A [Similar Products]
UniProt Entry Name
ACY1A_RAT
NCBI Summary for ACY1A
enzyme that displays aminoacylase and/or metallopeptidase functions; may be involved in amino acid metabolism [RGD, Feb 2006]
UniProt Comments for ACY1A
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 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; Hydrolase; EC 3.5.1.14
Cellular Component: cytoplasm
Molecular Function: aminoacylase activity; metal ion binding; metallopeptidase activity
Biological Process: amino acid metabolic process; protein catabolic process; proteolysis
Research Articles on ACY1A
1. These findings proposed ACY 1 as a new marker transcript for absorbing cells of intestinal crypt, which can be used to monitor the process of intestinal N-alpha-acetylated protein metabolism.[ACY 1]
Precautions
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Disclaimer
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