| Catalog: | C-FC-3609A | 
| Product Type: | FCM Antibody | 
| Size: | 50 µL/100 µL | 
| Reactivity: | Human | 
| Specificity: | Human Aminoacylase 1 | 
| Analysis mode: | FCM,ICC/IF | 
| Host: | Rabbit | 
| Clonality: | Monoclonal | 
| Isotype: | IgG | 
| Alternate names: | aminoacylase 1 | 
| Form: | Liquid | 
| Shipping: | This antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | 
| 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. | 
| Purification method: | Protein A | 
| Conjugation: | Unconjugated | 
| Immunogen: | Recombinant Human ACY1 / Aminoacylase-1 protein | 
| Buffer: | 0.2 μm filtered solution in PBS | 
Aminoacylase 1 (ACY1), a metalloenzyme that removes amide-linked ACY1 groups from amino acids and may play a role in regulating responses to oxidative stress. Both the C-terminal fragment found in the two-hybrid screen and full-length ACY1 co-immunoprecipitate with SphK1. Though both C-terminal and full-length proteins slightly reduce SphK1 activity measured in vitro, the C-terminal fragment inhibits while full-length ACY1 potentiates the effects of SphK1 on proliferation and apoptosis. It suggested that ACY1 physically interacts with SphK1 and may influence its physiological functions. As a homodimeric zinc-binding enzyme, Aminoacylase 1 catalyzes the hydrolysis of N alpha-acylated amino acids. Deficiency of Aminoacylase 1 due to mutations in the Aminoacylase 1 (ACY1) gene follows an autosomal-recessive trait of inheritance and is characterized by accumulation of N-acetyl amino acids in the urine.
Copyright © 2025 Creative Biogene. All rights reserved.