|Related Categories||3.x.x.x Hydrolases, Biochemicals and Reagents, Chemical Synthesis, Enzyme Class Index, Enzyme Kits,|
96667 Esterase from Bacillus subtilis, 10 mg
51963 Esterase from Bacillus subtilis, 10 mg
46051 Esterase from Bacillus stearothermophilus, 10 mg
79208 Esterase from Rhizopus oryzae, 100 mg
46056 Esterase from Candida lipolytica, 50 mg
46059 Esterase from Mucor miehei, 50 mg
46069 Esterase from horse liver, 50 mg
46071 Esterase from Saccharomyces cerevisiae, 25 mg
46058 Esterase from hog liver, 10 mg
75742 Esterase Pseudomonas fluorescens, recombinant from E. coli, 10 mg
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Kit formulated with all liquid reagents.
lyophilized, powder, slightly beige, ≥50 U/mg
lyophilized powder, ≥15 units/mg solid
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Keywords: Cell culture, Cell disruption, Cell signaling, Diagnostic, Digestions, Drug discovery, Functional genomics, Gene expression, Genomics, Metabolic Pathways, Molecular biology, Neuroscience, Proteomics
Impact of induced fit on ligand binding to the androgen receptor: a multidimensional QSAR study to predict endocrine-disrupting effects of environmental chemicals. Markus A Lill et al J. Med. Chem. 48, 5666-74, (2005)
Neurosteroid analogues. 11. Alternative ring system scaffolds: gamma-aminobutyric acid receptor modulation and anesthetic actions of benz[f]indenes. Jamie B Scaglione et al J. Med. Chem. 49, 4595-605, (2006)
Neurosteroid analogues. 14. Alternative ring system scaffolds: GABA modulatory and anesthetic actions of cyclopenta[b]phenanthrenes and cyclopenta[b]anthracenes. Jamie B Scaglione et al J. Med. Chem. 51, 1309-18, (2008)
Novel potent and selective bile acid derivatives as TGR5 agonists: biological screening, structure-activity relationships, and molecular modeling studies. Hiroyuki Sato et al J. Med. Chem. 51, 1831-41, (2008)
Potent and selective steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 7, an enzyme that catalyzes the reduction of the key hormones estrone and dihydrotestosterone. Edith Bellavance et al J. Med. Chem. 52, 7488-502, (2009)
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