• The enzyme cholesterol esterase hydrolyses the (S)-diester but not the (R)-diester. (wikipedia.org)
  • Those cells were focally positive for naphthol AS-D chloroacetate esterase. (bvsalud.org)
  • Telogorejo dan RS Elisabeth dengan menggunakan pengecatan Giemsa dan Mieloperoksidase ( MPO ) , Naphthol AS-D Chloroacetate ( CLE ), a - Naphthyl Butyrate Esterase ( BUE ) dan imunositokimia Terminal Deoxynucleotidyl Transferase ( TdT. (undip.ac.id)
  • A combined cytochemical and biochemical analysis of non-specific esterases in differentiating root tissues of the broad bean showed that maximal enzyme activity, expressed on a per segment, per unit protein or per unit area of average-sized section basis, occurred within the zone of cell expansion, elongation and differentiation of procambial tissues. (gre.ac.uk)
  • In a study of non-specific esterases in soft fruit ripening and senescence, cytochemical studies demonstrated that enzyme activity was associated with subcellular structures in the pulp cells of the ripening strawberry. (gre.ac.uk)
  • Enzyme activities are expressed Inhibitors,Modulators,Libraries as nmole of naphthol or B naphthol min mg protein. (srcinhibitors.com)
  • Distribution of T-lymphocytes in follicular lymphomas as revealed by acid alpha-naphthol acetate esterase. (bmj.com)
  • Twelve cases of follicular centroblastic/centrocytic malignant lymphoma were studied for acid non-specific esterase. (bmj.com)
  • Three study locations (Djougou, Gogounou and Kandi) showed high oxidase activity and four sites (Djougou, Ouake, Copargo and Kandi) showed elevated esterase activity. (biomedcentral.com)
  • Using the histochemical reagents, naphthol AS D acetate and the diazonium salt, fast red violet LB salt, a biochemical study of non-specific esterases extracted from broad bean root tips, has shown that these enzymes have an estimated Km of 0.07 mM, a pH optimum of 5.5 and that they lose substantial activity when dialysed against distilled water as opposed to 5mM magnesium chloride and 10mM phosphate buffer. (gre.ac.uk)
  • Although esterase activity changed little during the transition from 'maturing 1 to 'mature 1 when expressed on either basis, the specific activity of the enzymes fell markedly. (gre.ac.uk)
  • The activity against each substrate was calculated from standard curves of absorbance for known concentrations of naphthol or B naphthol. (srcinhibitors.com)
  • 1961). Among workers engaged in the production, handling and shipping of carbaryl, those most heavily exposed (air concentrations of 0.23 to 31 mg/M 3 ) excreted large amounts of total 1-naphthol (Best & Murray, 1962). (inchem.org)
  • Statistical analyses of histochemical data have shown that particles staining for naphthol AS BI phosphatase in dividing unfixed root cells of Vicia f aba do not act as a 'trigger 1 in the way suggested for animal cells, since there were significantly greater numbers of particles in mitotic cells as opposed to interphase cells in all 3 root tissues, apical initials, procortex and central cylinder. (gre.ac.uk)
  • Histological staining techniques have revolutionized our understanding of cellular processes, and the α-Naphthyl Acetate Esterase (α-NAE) stain holds a significant place in this field. (pscientifics.com)
  • The α-Naphthyl Acetate Esterase (α-NAE) stain offers a fascinating glimpse into cellular esterase activity. (pscientifics.com)
  • In the blast cells of all ALL cases myeloperoxi- dase, Sudan Black B and naphtol ASD chloroacetate esterase are claimed to be negative (Shaw, 1976). (swirlzcupcakes.com)
  • We also assessed the sublethal effects of Proclaim Fit ® on the specific activity of some well-known detoxifying enzymes including α-esterase, β-esterase, and Glutathione S-transferase (GST) in the honey bees. (researchsquare.com)
  • Enzyme assays revealed the considerable involvement of the enzymes, especially GST and α-esterase, in detoxification of the Proclaim Fit ® , but their activities were significantly influenced by route of exposure and age of bee. (researchsquare.com)
  • Esterases (ESTs) are the enzymes involved in Phase I xenobiotic detoxification reactions that degrade toxins via hydrolysis (Xu et al. (researchsquare.com)
  • 2013). These hydrolytic enzymes are divided into alpha (α) and beta (β) esterases depending on their ability to hydrolyze the substrates alpha- and beta-naphthyl, respectively (Dahan-Moss and Koekemoer 2016). (researchsquare.com)
  • This technique is referred to as "Non-specific Esterase Stain" due to its lack of specificity toward esterases. (pscientifics.com)