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NAAA encodes an N-acylethanolamine-hydrolyzing enzyme which is highly similar to acid ceramidase. Additionally we are shipping NAAA Proteins (11) and NAAA Kits (9) and many more products for this protein.
Showing 10 out of 45 products:
Cow (Bovine) Polyclonal NAAA Primary Antibody for IHC, WB - ABIN2782073
Schulze, Schepers, Sandhoff: Overexpression and mass spectrometry analysis of mature human acid ceramidase. in Biological chemistry 2007
Show all 2 Pubmed References
Variants a1 and a2 encoded the same full-length NAAA protein.
The results suggest that N-acylethanolamine acid amidase and protein tyrosine kinase 7 (show PTK7 Antibodies) may be used as potential tissue biomarkers to avoid overtreatment of non-aggressive prostate cancer
MALDI-TOF (show FEZF2 Antibodies) MS analysis of the human NAAA zymogen (47.7 kDa) treated with peptide-N-glycosidase F (PNGase (show NGLY1 Antibodies) F) identified 4 glycosylation sites, and acid cleavage of the zymogen into alpha- and beta-subunits (14.6 and 33.3 kDa) activated the enzyme.
The level and activity of acid ceramidase (show ASAH1 Antibodies) in Alzheimer disease (AD) brain may play a role in controlling neuronal apoptosis and may mediate signalling pathways involved in the molecular mechanism of AD.
we describe the overexpression and processing of recombinant human acid ceramidase (show ASAH1 Antibodies) in insect cells, its purification and characterization
These results showed that both N-acylethanolamine-hydrolysing acid amidase (show GATA1 Antibodies) and fatty acid amide hydrolase (show FAAH Antibodies) are functionally active in human prostate cancer cells.
Both inhibitors reduced several markers of macrophage activation, such as mRNA expression of inflammatory mediators, as well as cytokine and prostaglandin production, with however some differences between FAAH (show FAAH Antibodies) and NAAA inhibition. Our results support an important role for inhibition of NAE hydrolysis and NAAA inhibition in particular in controlling macrophage activation, and thus inflammation.
NAAA inhibition increases palmitoylethanolamide levels in the colon and reduces colon inflammation and systemic inflammation
NAAA regulates peripheral pain initiation by interrupting endogenous fatty acid ethanolamide signaling at PPAR-alpha (show PPARA Antibodies).
Results suggest that N-acylethanolamine-hydrolyzing acid amidase and fatty acid amide hydrolase (show FAAH Antibodies) cooperatively degrade anandamide and other N-acylethanolamines in macrophages.
This gene encodes an N-acylethanolamine-hydrolyzing enzyme which is highly similar to acid ceramidase. Multiple transcript variants encoding different isoforms have been found for this gene.
N-acylsphingosine amidohydrolase (acid ceramidase)-like
, N-acylethanolamine acid amidase
, N-acylsphingosine amidohydrolase-like protein
, N-acylethanolamine-hydrolyzing acid amidase-like
, n-acylethanolamine-hydrolyzing acid amidase-like
, ASAH-like protein
, N-acylethanolamine-hydrolyzing acid amidase
, acid ceramidase-like protein