Aminoacylase 1 (ACY1) Mouse Monoclonal Antibody [Clone ID: AT1E2]
CAT#: AM50353PU-N
Aminoacylase 1 (ACY1) mouse monoclonal antibody, clone AT1E2, Purified
Size: 50 ul
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CNY 6,620.00
货期*
5周
规格
Specifications
Product Data | |
Clone Name | AT1E2 |
Applications | ELISA, WB |
Recommend Dilution | The antibody has been tested by ELISA, Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended starting dilution is 1:1000. |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Recombinant human ACY1 (1-408aa) purified from E. coli. |
Formulation | PBS, pH 7.4 containing 0.02% Sodium Azide and 10% Glycerol State: Purified State: Liquid purified Ig fraction |
Concentration | lot specific |
Purification | Protein-A affinity chromatography |
Conjugation | Unconjugated |
Storage Condition | Store undiluted at 2-8°C for up to two weeks or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
Gene Name | aminoacylase 1 |
Database Link | |
Background | Aminoacylase-1, also designated N-acyl-L-amino-acid amidohydrolase or ACY1, is a member of the largest metallopeptidase family called M20A. Aminoacylase-1 is a zinc-binding homodimeric enzyme expressed in kidney, brain, placenta and spleen. It is the most abundant of the aminoacylases. 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. All affected individuals exhibit markedly increased urinary excretion of several N-acetylated amino acids. |
Synonyms | ACY-1 |
Reference Data | |
Protein Families | Protease |
Protein Pathways | Arginine and proline metabolism, Metabolic pathways |
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